Intellectual Property Rights and International
International Trade
Shayerah Ilias
Analyst Akhtar
Specialist in International Trade and Finance
Ian F. Fergusson
Specialist in International Trade and Finance
February 17, 2011April 4, 2014
Congressional Research Service
7-5700
www.crs.gov
RL34292
CRS Report for Congress
Prepared for Members and Committees of Congress
Intellectual Property Rights and International Trade
Summary
This report provides background on intellectual property rights (IPR) and discusses the role of
U.S. international trade policy in enhancing IPR protection and enforcement abroad. IPR are legal
rights granted by governments to encourage innovation and creative output by ensuring that
creators reap the benefits of their inventions or works, and they may take the form of patents,
trade secrets, copyrights, trademarks, or geographical indications. U.S. industries that rely on IPR
contribute significantly to U.S. economic growth, employment, and trade with other countries.
Counterfeiting and piracy in other countries may result in the loss of billions of dollars of revenue
for U.S. firms as well as the loss of U.S. jobs. Responsibility for developing IPR policy, engaging
in IPR-related international negotiations, and enforcing IPR laws cuts across several different
U.S. government agencies.
Promoting the enforcement of IPR is an important component of U.S. international trade policy.
Since the 1995 Agreement on Trade-Related Aspects of Intellectual Property Rights (TRIPS
Agreement) at the World Trade Organization (WTO), trade policy has been used to promote
enforcement of IPR abroad. The United States and several trading partners have been negotiating
the Anti-Counterfeiting Trade Agreement (ACTA), which would surpass TRIPS Agreement
commitments.
The United States also pursues international IPR support through regional and bilateral free trade
agreements (FTAs), which often include IPR commitments by U.S. partners exceeding their
TRIPS Agreement obligations. However, the May 10, 2007 bipartisan trade agreement led to a
scale-back of some of the IPR requirements in the Peru, Panama and Colombia FTAs, in an effort
to bolster bipartisan support for the FTAs. Other trade policy tools also are available for U.S.
efforts to advance international IPR. Pursuant to Section 182 of the Trade Act of 1974 as
amended (P.L. 93-618), the Office of the U.S. Trade Representative (USTR) identifies countries
providing inadequate IPR protection in its annual “Special 301” report. Section 337 of the
amended Tariff Act of 1930 authorizes the U.S. International Trade Commission (ITC) to prohibit
U.S. imports of infringing products. Additionally, under the Generalized System of Preferences
(GSP), the United States may consider a developing country’s IPR policies and practices as a
basis for offering or suspending preferential duty-free entry to certain products from the country.
IPR protection and enforcement has been a focal point of legislative activity in recent sessions of
Congress. In the 110th Congress, legislation was enacted to establish a new entity to coordinate
intellectual property activities within the federal government (P.L. 110-403). In the 111th
Congress, legislation was introduced calling for greater U.S. international IPR enforcement
efforts and increased prioritization of resources devoted to such activities (H.R. 496 and related
bill S. 1466; H.R. 2410 and H.R. 2475).
Given the role of IPR in the U.S. economy and its contribution to U.S. employment and trade,
IPR issues related to international trade policy may figure prominently in the 112th congressional
agenda. Congress may choose to consider whether or not FTAs are an appropriate vehicle for
boosting intellectual property protection and enforcement. Congress also may balance IPR
protection and enforcement with other public policy goals such as access to medicine in poor or
developing countries. In addition, Congress may examine the effectiveness of the current U.S.
coordinating structure for promoting international IPR support.
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Intellectual Property Rights and International Trade
Contents
Introduction ................................................................................................................................6
Intellectual Property Rights Basics ..............................................................................................6
Types of IPR .........................................................................................................................6
Patents ............................................................................................................................6
Trade Secrets ..................................................................................................................7
Copyright........................................................................................................................7
Trademarks .....................................................................................................................8
Infringement of IPR ..............................................................................................................8
Piracy .............................................................................................................................8
Counterfeiting.................................................................................................................9
Global Intellectual Property Holdings..........................................................................................9
Contribution of Intellectual Property to U.S. Economy .............................................................. 10
Prevalence and Economic Consequences of IPR Infringement............................................. 12
Seizures ........................................................................................................................ 12
Sectoral Infringement.................................................................................................... 14
Limitations on Data Estimating IPR Infringement Costs...................................................... 16
The Organization Structure of IPR Protection............................................................................ 17
Multilateral IPR System ...................................................................................................... 17
World Trade Organization (WTO) ................................................................................. 17
Declaration on TRIPS Agreement and Public Health .................................................... 19
World Intellectual Property Organization (WIPO) ......................................................... 21
Free Trade Agreements ....................................................................................................... 24
Trade Promotion Authority and Negotiating Objectives ................................................. 24
Current IPR-Related U.S. FTA Activity ......................................................................... 25
Central IPR Standards in U.S. FTAs .............................................................................. 26
U.S. Trade Law ......................................................................................................................... 31
Special 301 ......................................................................................................................... 31
Special 301 Country Lists ............................................................................................. 32
Country Identification Factors....................................................................................... 33
Section 337 ......................................................................................................................... 34
Generalized System of Preferences...................................................................................... 35
U.S. Agency Functions and Funding for IPR ....................................................................... 35
Department of Commerce (Commerce) ......................................................................... 36
Department of Justice (DOJ) ......................................................................................... 37
Department of Homeland Security (DHS) ..................................................................... 37
Food and Drug Administration (FDA) ........................................................................... 38
Copyright Office ........................................................................................................... 38
Department of State (State) ........................................................................................... 38
U.S. Agency for International Development (AID) ........................................................ 39
United States Trade Representative (USTR) .................................................................. 39
United States International Trade Commission (ITC)..................................................... 39
Intellectual Property Enforcement Coordinator (IPEC) .................................................. 40
Issues for Congress ................................................................................................................... 40
U.S. Efforts to Promote IPR Through Trade Policy.............................................................. 41
Effectiveness of the U.S. IPR Organizational Structure........................................................ 42
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Figures
Figure 1. Border Seizures of Counterfeit and Pirated Goods: FY2009........................................ 13
Figure 2. Estimated Software Piracy Rates in Selected Countries and Estimated Related
Software Piracy Losses to U.S. Businesses ............................................................................. 15
Tables
Table 1. Global Intellectual Property Filings Through the PCT, 2006-2009..................................9
Table 2. Estimated Damages for PhRMA Member Companies From Data Exclusivity and
Patent Protection Violations ................................................................................................... 16
Table 3. Summary of WIPO-Administered IPR Treaties ............................................................ 22
Table 4. Patent and Copyright Provisions in the TRIPS Agreement and U.S. FTAs .................... 29
Contacts
Author Contact Information ...................................................................................................... 43
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Introduction
Intellectual property rights (IPR) traditionally have been matters of national concern. Individual
nation states have developed IPR regimes reflecting their domestic needs and priorities. Over
time, intellectual property protection and enforcement have come to the forefront as a key
international trade issue for the United States, figuring prominently in the multilateral trade policy
arena and in regional and bilateral U.S. free trade agreements (FTAs).
The protection and enforcement of IPR in the United States and abroad is of key interest to
Congress. Intellectual property is an increasingly critical component of the U.S. economy.
Industries that rely on intellectual property protection in the United States claim to lose billions of
dollars each year due to overseas IPR infringement. In light of the recent international financial
crisis and global economic downturn, congressional interest has grown in the role of IPR in
advancing U.S. industrial competitiveness and contributing to U.S. economic recovery following
the recent international crisis. Members of Congress also have expressed concern about the
potential health and safety consequences of counterfeit pharmaceutical drugs and other products,
as well as the possible link between terrorist groups and traffic in counterfeit and pirated goods.
This report discusses the different kinds of IPR and forms of IPR infringement; importance of
IPR to the U.S. economy; estimated losses associated with IPR infringement; organizational
structure of IPR protection in multilateral, regional, bilateral arenas; U.S. government agencies
involved with IPR and trade; and issues for Congress regarding IPR and international trade.
Intellectual Property Rights Basics
This section provides definitions of the various kinds of intellectual property rights (patents, trade
secrets, copyrights, trademarks, and geographical indications) and intellectual property rights
misappropriation (infringement, piracy, and counterfeiting).
Types of IPR
IPR are legal rights granted by governments to encourage innovation and creative output. They
ensure that creators reap the benefits of their inventions or works and may take the form of
patents, trade secrets, copyrights, trademarks, or geographical indications. Through IPR,
governments grant a temporary legal monopoly to innovators by giving them the right to limit or
control the use of their creations by others. IPR may be traded or licensed to others, usually in
return for fees and or royalty payments. Although the World Trade Organization (WTO)
Agreement on Trade-Related Aspects of Intellectual Property Rights (TRIPS) provides minimum
standards for IPR protections, such rights are granted on a national basis and are, in general,
enforceable only in the country in which they are granted. However, countries are obliged to
abide by WTO rules and their IPR enforcement practices can be challenged by other countries at
the WTO.
Patents
The Patent Act (35 U.S.C. 101 et seq) governs the issuance and use of patents in the United
States. Patents are granted for inventions of new products, processes, or organisms (known as
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utility patents). Patents also may be granted for designs and plants. For an invention to be
patentable, it must be new, “non-obvious” (involving an inventive step), and have a potential
industrial or commercial application. The patent provides the holder with the exclusive right to
sell the invention for a period of 20 years, or to prevent the incorporation of the invention into
other products without the permission of the rights-holder. The patent right is based on the
proposition that inventors must be granted a temporary monopoly over their invention in order to
encourage innovation and to promote the expenditure of money on research and development.
The patent holder recoups these up-front costs through a temporary monopoly over sale of the
invention. In return for this economic rent, the patent holder must disclose the content of the
patent along with test data and other information concerning the invention. This is meant to spur
further creativity by those seeking to build on the patent after its expiration. Domestically, patents
are granted by the Patent and Trademark Office (PTO) of the Department of Commerce.
Trade Secrets
A trade secret is any type of valuable information, including a “formula, pattern, compilation,
program device, method, technique, or process,” that derives independent economic value from
not being generally known or readily ascertainable and is subject to reasonable efforts by the
owner to maintain its secrecy.1 Examples of trade secrets include blueprints, customer lists, and
pricing information. While protection of patents and copyright is a matter of federal law, trade
secret protection is found also in state law. However, most states subscribe to the Uniform Trade
Secret Act (UTSA).
There are important differences between trade secrets and patents. Individuals do not have to
apply for trade secret protection as they would for patents. Protection of trade secrets originates
immediately with the creation of the trade secret; there is no process for applying for or
registering trade secrets. Trade secret protection does not expire unless the trade secret becomes
known. In contrast, patent applicants must disclose information about their innovation to the PTO
in order to acquire a patent. Patents offer rights holders stronger protection but for a limited
period of time. While applying for a patent can be a costly and lengthy process, patents are
valuable if the confidentiality of the innovation is fragile or if the area of research is highly
competitive.
Copyright
Protection of copyrights in the United States is based on the Copyright Act (17 U.S.C. 101, et
seq). Copyrights protect original expressions of authorship. Such protections include literary or
artistic works such as books, music, sound recordings, movies, paintings, architectural works, and
computer software and databases (though not individual bits of data). Traditionally, copyrights
differed from patents in that there was no claim to industrial applicability or novelty of the idea.
The expression of the idea, not the underlying idea, was being copyrighted. While some of the
criteria for copyrights differ from those of patents, the objective is the same: investments of time,
money, and effort to create work of cultural, social and economic significance should be protected
to encourage further creativity. U.S. law protects authorship for life plus 70 years for personal
works, or 120 years from creation (or 95 years from publication) for corporate works. Copyrights
1
Uniform Trade Secret Act, §1(4).
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may be registered by the Copyright Office of the Library of Congress, or acquired through
creating and fixation of the work of authorship.
Trademarks
Trademark protection in the United States is governed jointly by state and federal law. The main
federal statute is the Lanham Act of 1946 (15 U.S.C. 1051, et seq). Also known as service marks,
trademarks permit the seller to use a distinctive name, mark, or symbol to identify and market a
product, service, or company. The trademark allows quick identification of the seller’s product,
and for good or ill, can become an indicator of a product’s quality. If for good, the trademark can
be valuable in the introduction of new products by conveying an instant assurance of quality. The
trademark is designed to prevent other companies with similar merchandise from free-riding on
the association of quality with the trademarked item. Thus, a trademarked good may command a
premium in the marketplace because of its reputation. For trademarks, distinctiveness is at a
premium because a trademark must capture the consumer’s imagination to be effective as generic
names of commodities cannot be trademarked. Trademark rights are acquired through use or
through registration with the PTO.
A related concept to trademarks is the geographic indication, which is also protected by the
Lanham Act. The geographic indication acts to protect the quality and reputation of a distinctive
product originating in a certain region; however, the benefit does not accrue to a sole producer,
but rather the producers of a region. Geographic indications are generally sought for agricultural
products, or wines and spirits. Protection for geographical indications is acquired in the United
States by registration with the PTO, through a process similar to trademark registration.2
Infringement of IPR
IPR infringement is the misappropriation or violation of the IPR. In the case of patents,
infringement of a patent owner’s exclusive rights (as afforded by patent laws) involves a third
party’s unauthorized use of the patented device. As relates to international trade, the greatest
challenge to the patent right is infringement in foreign countries, or non-observance by WTO
member states to the minimal standards of the TRIPS Agreement. Copyright infringement occurs
when a third party engages in reproducing, performing, making sound or visual recordings of, or
broadcasting a copyrighted work without the consent of the copyright owner.
Piracy
The term “piracy” has applications to both copyrights and trademarks. The major challenge
facing copyright protection is piracy, either through physical duplication of the work, illegal
dissemination of copyrighted material (such as computer software, music, or movies) over the
Internet, and/or participation in commercial transactions of copyrighted materials without the
consent of the copyright owner. With respect to trademarks, piracy involves the registration or use
of a famous foreign trademark that is not registered in the country or is invalid because the
trademark has not been used.
2
For information on geographical indications and international trade negotiations, see CRS Report RS21569,
Geographical Indications and WTO Negotiations, by Charles E. Hanrahan.
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Counterfeiting
An imitation of a product is referred to as a “counterfeit” or a “fake.” Counterfeit products are
manufactured, marketed, and distributed with the appearance of being the genuine good and
originating from the genuine manufacturer.3 The purpose of counterfeit goods is to deceive
consumers about their origin and nature. Counterfeiting and copying of original goods are major
challenges for trademarked products. The counterfeited product can be sold for a premium
because of its association with the original item, while reducing the sales of the original items.
Furthermore, consumer experience with a counterfeited good of inferior quality, can damage the
reputation of the trademark product. Popular examples of counterfeit products in fake
fashionwear, such as Louis Vuitton bags or Rolex watches, or fake pharmaceutical products, such
as popular brand-name prescription medicines.
A related issue is the imitation of labels and packaging of trademarked goods. In this situation, the
imitator uses a trademark that is confusingly similar to a well-known trademark in order to
benefit from the reputation of the product with which he is competing.
Global Intellectual Property Holdings
The total number of patent filing applications received under the Patent Cooperation Treaty
(PCT), an international patent filing system administered by the World Intellectual Property
Organization (WIPO), has grown in recent years. After peaking in 2008, international patent
filings under the PCT fell by 4.5% in 2009, reflecting the international financial crisis. The
contraction of the global economy has been associated with a decline in investment and spending
on research and development.4 In 2010, international patent filings grew by 4.8% to 162,900—
nearly 2008 levels (see Table 1). 5
Intellectual property holdings that are protected by international agreements are highly
concentrated in certain countries. The United States continues to be the source of the world’s
largest number of patent filing applications under the PCT, accounting for nearly one-third of
such filings in 2010. However, the U.S. growth rate of patent filings has been negative in recent
years. The United States, along with Germany and Japan, accounted for about 60% of all patent
applications filed in 2010 under the PCT. China ranked as the fourth largest source of
international patent filings under the PCT in 2010, representing about 8% of global filings. China
had the highest growth rate in such filings, at about 56% in that year.
Table 1. Global Intellectual Property Filings Through the PCT, 2006-2009
Country
2008
2009
Filings
Filings
2010
Filings
Percent of
Growth from
3
Counterfeit goods should be distinguished from generic goods, i.e., in the case of generic forms of pharmaceutical
medicines.
4
WIPO, "Global Economic Slowdown Impacts 2008 International Patent Filings," press release, January 27, 2009,
http://www.wipo.int/pressroom/en/articles/2009/article_0002.html.
5
WIPO, "International Patent Filings Recover in 2010," press release, February 9, 2011,
http://www.wipo.int/pressroom/en/articles/2011/article_0004.html.
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Country
2008
2009
2010
Total
Previous Years
United States
51,637
45,618
44,855
27.5%
-1.7%
Japan
28,760
29,802
32,156
19.7%
7.9%
Germany
18,855
16,797
17,171
10.5%
2.2%
China
6,120
7,900
12,337
7.6%
56.2%
South Korea
7,899
8,035
9,686
5.9%
20.5%
France
7,072
7,237
7,193
4.4%
-0.6%
United Kingdom
5,466
5,044
4,857
3.0%
-3.7%
Netherlands
4,363
4,462
4,097
2.5%
-8.2%
Switzerland
3,799
3,671
3,611
2.2%
-1.6%
Sweden
4,137
3,567
3,152
1.9%
-11.6%
Canada
2,976
2,527
2,707
1.7%
7.1%
Italy
2,883
2,652
2,632
1.6%
-0.8%
Finland
2,214
2,123
2,076
1.3%
-2.2%
Australia
1,938
1,740
1,736
1.1%
-0.2%
Spain
1,390
1,564
1,725
1.1%
10.3%
13,725
12,659
12,909
7.9%
2.0%
163,234
155,398
162,900
All Others
Total
Source: World Intellectual Property Organization.
Contribution of Intellectual Property to U.S.
Economy
Intellectual property is an important source of comparative advantage for the United States.
Nearly every industry depends on IPR for its businesses. Among the industries that are dependent
on patent protection are the aerospace, automotive, computer, consumer electronics,
pharmaceutical, and semiconductor industries. Copyright-based industries include the software,
data processing, motion picture, publishing, and recording industries. Other industries that
indirectly benefit from IPR protection include retailers, traders, and transportation businesses,
which support the distribution of goods and services derived from intellectual property.6
The role of IPR in the U.S. economy has been longstanding. Some evidence suggests that factors
linked to innovation account for about three-fourths of the United States’ post-World War II
growth rate.7 In recent years, the role of IPR in the U.S. economy has grown. Various studies
6
Stephen E. Siwek, “Engines of Growth: Economic Contributions of the US Intellectual Property Industries,”
commissioned by NBC Universal, 2005, p. 2.
7
Arti Rai, Stuart Graham, and Mark Doms, Patent Reform: Unleashing Innovation, Promoting Economic Growth &
Producing High-Paying Jobs, Department of Commerce, A White Paper from the U.S. Department of Commerce,
(continued...)
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suggest that IP-related industries are one of the largest source of jobs in the United States. One
study using data from 2000-2007 found that, among tradable industries, IP-intensive industries
surpass non-IP-intensive industries on a range of economic measures, including job creation,
wages, output and sales per employee, and exports. During this time period, according to the
study, IP-intensive industries paid both their low- and highly skilled employees close to 60%
more than non-IP-intensive industries. The report also found that IP-intensive industries
represented nearly 60% of total U.S. exports during 2000-2007.8 More broadly, IPR-intensive
industries may contribute positively to the U.S. economy through productivity gains and other
spillover effects.
Industry-specific figures may further demonstrate the importance of IP to the U.S. economy. For
example, in 2007, the business and entertainment software, motion picture, recording, and
publishing industries, which rely on copyright protection, were estimated to contribute about
$889 billion to the U.S. economy (“value-added” to current GDP), or about 6.44% of the U.S.
economy. This was an increase from 2006, during which the value-added of these copyright
industries to the U.S. GDP totaled $837 billion, or 6.35% of the U.S. economy. These copyright
industries also accounted for nearly 23% of real U.S. annual economic growth in 2007, up from
about 13% in 2006. In terms of U.S. employment, the copyright industries represented 4% of U.S.
workers (5.6 million workers) in 2007, similar to the prior year. Foreign sales and exports from
these industries amounted to $126 billion in 2007, up from $116 billion in 2006.9
The pharmaceutical industry, which is patent-intensive, provides another illustration of
intellectual property contributions to the U.S. economy. In 2009, domestic sales by researchbased pharmaceutical companies that are members of Pharmaceutical Researchers and
Manufacturers of America (PhRMA) reached an estimated $183 billion, while sales abroad by
PhRMA member companies totaled about $103 billion.10
The intellectual property industries contribute positively to the overall U.S. trade balance through
royalties and licensing fees. Rights-holders may authorize the use of technologies, trademarks,
and entertainment products that they own to entities in foreign countries, resulting in revenues
through royalties and license fees. 11 In 2009, U.S. receipts from cross-border trade in royalties
and license fees (relating to patent, trademark, copyright, and other intangible rights) totaled
$89.8 billion, down from $93.9 billion in the previous year. Also in 2009, U.S. payments of
royalties and license fees to foreign countries amounted to $25.2 billion, down from $25.8 billion
in the year before. Industrial processes, computer software, and trademarks accounted for the bulk
of U.S. international trade in intangible assets.12
(...continued)
April 13, 2010.
8
Nam D. Pham, The Impact of Innovation and the Role of Intellectual Property Rights on U.S. Productivity,
Competitiveness, Jobs, Wages, and Exports, NDP Consulting Group, April 2010.
9
Stephen E. Siwek, Copyright Industries in the U.S. Economy: The 2003-2007 Report, prepared for the International
Intellectual Property Alliance (IIPA), http://www.iipa.com, pp. 3-7.
10
PhRMA, Pharmaceutical Industry Profile 2010, Washington, D.C., March 2010, http://www.phrma.org, p. 50.
11
Amanda Horan, Christopher Johnson, and Heather Sykes, Foreign Infringement of Intellectual Property Rights:
Implications for Selected U.S. Industries, U.S. International Trade Commission, Office of Industries Working Paper,
October 2005, p. 4.
12
Jennifer Koncz and Anne Flatness, “U.S. International Services,” Survey of Current Business, U.S. Bureau of
Economic Analysis (BEA), October 2010. This measure of cross-border trade in royalties and license fees by U.S.
companies include transactions with both affiliated and unaffiliated foreign companies.
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Some advocates of civil liberties assert that empirical analysis on the role of IPR in the U.S.
economy may not be fully evaluating the economic and commercial benefits of lawful exceptions
and limitations to exclusive rights. For example, by one estimate, businesses that rely on “fair
use” exceptions to U.S. copyright law contribute $2.2 trillion to the U.S. economy. The “fair use”
doctrine permits limitations and exceptions to the exclusive right afforded by copyright law. It
permits limited use of copyrighted works without requiring permission from the right holder in
certain cases, examples of which may include news reporting, research, teaching, and library
use. 13
Prevalence and Economic Consequences of IPR Infringement
Advances in information and technology and declining costs of transportation and
communication, spurred by globalization, have fundamentally changed information and trade
flows. Such changes have created new markets for U.S. exporters, but at the same time, have
been associated with the proliferation of counterfeiting and piracy on a global scale.
Several factors contribute to the growing problem of IPR infringement. While the costs and time
for research and development are high, IPR infringement is associated with relatively low costs
and risks and a high profit margin. According to PhRMA, it takes a pharmaceutical company
about 10 to 15 years of research and development to create a new drug. PhRMA member
companies collectively spent an estimated $46 billion for research and development (domestic
and abroad) in 2009.14 In contrast, drug counterfeiters can lower production costs by using
inexpensive, and perhaps dangerous or ineffective, ingredient substitutes.
The development of technologies and products that can be easily duplicated, such as recorded or
digital media, also has led to an increase in counterfeiting and piracy. Increasing Internet usage
has contributed to the distribution of counterfeit and pirated products. Additionally, civil and
criminal penalties often are not sufficient deterrents for piracy and counterfeiting. The United
States is especially concerned with foreign IPR infringement of U.S. intellectual property.
Compared to foreign countries, IPR infringements levels in the United States are estimated to be
relatively low.
Seizures
Because of the secretive, illicit nature of IPR infringement, it is difficult to estimate the
magnitude of its impact on U.S. producers and exporters. However, customs data on seizures of
counterfeit and pirated goods may offer some idea of the magnitudes involved. One study by the
Organization for Economic Cooperation and Development (OECD) indirectly extrapolated
available customs data on seizures to conclude that world trade in counterfeit and pirated goods
may have amounted to about $200 billion in 2005. In particular, the study used the customs
information to estimate the probability that imports of particular goods from particular countries
would be pirated or counterfeit. The OECD estimate does not include the counterfeit and pirated
13
Thomas Rogers and Andrew Zamosszegi, Fair Use in the U.S. Economy:Economic Contribution of Industries
Relying on Fair Use, Prepared for the Computer & Communications Industry Association (CCIA), 2010. CCIA, "Fair
Use Doctrine Vital for All of Us," press release, November 18, 2009,
http://www.ccianet.org/index.asp?sid=5&artid=125&evtflg=False. See also CRS Report RL33631, Copyright
Licensing in Music Distribution, Reproduction, and Public Performance, by Brian T. Yeh.
14
Ibid., p. 2.
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goods produced and consumed within a country and does not include infringing goods distributed
over the Internet. If these figures were included, the trade estimate likely would be higher.15
Updated estimates from the OECD suggest that trade in IPR-infringing goods may have totaled
up to $250 billion in 2007. During that same time period, the share of counterfeiting and pirated
goods in world trade also is estimated to have increased—from 1.85% in 2000 to 1.95% in
2007.16
Data on pirated and counterfeit seizures of imports at the U.S. border shed light of the magnitude
of the issue in the U.S. context (see Figure 1). In FY2009, the Customs and Border Protection
(CBP) and Immigration and Customs Enforcement (ICE) agencies of the Department of
Homeland Security (DHS) made 14,841 IPR-related seizures, more than double the FY2005 level
of 8,022. Between FY2005-FY2008, the domestic value of IPR-related seizures grew by more
than 25% each year. The domestic value of seizures peaked at $272 million in FY2008 and then
dropped by 4% to about $261 million in FY2009.17
Figure 1. Border Seizures of Counterfeit and Pirated Goods: FY2009
Toys and
Electronic Games
2%
Jewelry
4%
Pharmaceuticals
4%
Media
4%
All Others
8%
Computer and
Hardware
5%
Handbags,
Watches and
Wallets, and
Parts
Backpacks
6%
Wearing Apparel 8%
8%
Footwear
39%
Consumer
Electronics
12%
Sources: U.S. Customs and Border Protection and U.S. Immigration and Customs Enforcement.
Of all U.S. trading partners, China continues to account for the majority of counterfeits
intercepted at the U.S. border. In FY2009, seizures of goods originating from China represented
15
OECD, The Economic Impact of Counterfeiting and Piracy, 2007, p. 4,
http://www.oecd.org/dataoecd/13/12/38707619.pdf.
16
Organization for Economic Cooperation and Development (OECD), The Economic Impact of Counterfeiting and
Piracy, 2007. OECD, Magnitude of Counterfeiting and Piracy of Tangible Products: An Update, November 2009.
17
U.S CBP and U.S. ICE, Intellectual Property Rights Seizure Statistics: FY2009, October 2010.
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79% of all seizures and $205 million in value. Other top trading partners from which IPRinfringing goods were seized include Hong Kong, India, Taiwan, and Korea. 18
A top priority for the CBP is seizing counterfeit imports that endanger the health and safety of
consumers, such as fake healthcare products, pharmaceutical products, and consumer electronics.
The total value of IPR-related seizures of commodities that represent potential safety and security
risks was $32 million in FY2009. Pharmaceutical goods were the top commodity posing safe and
security risks, accounting for 34% ($11 million in domestic value) of such commodities
intercepted at U.S. borders. Imports from China represented 62% of IPR-related goods that were
intercepted at U.S. borders and identified as presenting safety and security risks, followed by such
imports from India at 9%.19
Sectoral Infringement
U.S. industries that rely on IPR protection claim to lose billions of dollars in revenue annually
due to piracy and counterfeiting. In addition, beyond the direct losses faced by U.S. intellectual
property-based firms, the U.S. economy may face additional “downstream” losses from IPR
infringement. According to this view, counterfeiting and piracy losses to U.S. firms, for example,
also result in the loss of jobs that would have been created if the infringement did not occur,
which translates into lost earnings by U.S. workers. This, in turn, translates into lost tax revenues
for federal, state, and local governments from lost personal income, corporate income, and
production taxes.20
Attempts have been made in some economic sectors to quantify the IPR infringement levels and
related losses to legitimate U.S. businesses. Two intellectual property-based sectors that have
calculated the extent of infringement in their industries and related costs are copyrights and
pharmaceuticals. A discussion of estimated losses from these two sectors follows.
Copyright Industry
The International Intellectual Property Alliance (IIPA), a coalition of seven member associations
representing over 1,900 U.S. copyright-based companies, provides annual estimates of U.S. trade
loss associated with copyright infringements in selected countries.21 For 2009, IIPA estimated that
copyright piracy in 43 countries resulted in $14.3 billion in U.S. business software losses and
$1.4 billion in U.S. records and music losses. China was the leading culprit in terms of trade
losses due to copyright piracy, contributing to $3.4 billion in business software losses and $466
million in records and music losses to U.S. businesses. 22
18
Ibid.
Ibid.
20
There may be limitations on data estimating the impact of counterfeiting and piracy on the U.S. economy. Some
critics point out that many of the estimates for losses associated with IPR infringement are generated by industry
groups that may have self-interested motivations and hence, the negative effects may be exaggerated.
21
The IIPA member associations are: Association of American Publishers (AAP), Business Software Alliance (BSA),
Entertainment Software Alliance (ESA), Independent Film & Television Alliance (I.F.T.A.), Motion Picture
Association of America (MPAA), National Music Publishers’ Association (NMPA), and Recording Industry
Association of America (RIAA).
22
IIPA, IIPA 2009 “Special 301” USTR Decisions, issued June 30, 2009.
19
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There is not always a direct relationship between IPR infringement rates and the costs to U.S.
firms (see Figure 2). The size of a country’s market and U.S. industries’ access to the market
affect the extent to which infringement rates translate into costs to U.S. IPR-based industries.
Thus, estimated losses from IPR infringement may be lower in a country with high piracy rates
but a small market for the United States, compared to a country with lower piracy rates but a
bigger market for United States.
Figure 2. Estimated Software Piracy Rates in Selected Countries and Estimated
Related Software Piracy Losses to U.S. Businesses
Source: Business Software Alliance.
Notes: The countries listed were identified as Priority Watch List countries in the 2010 “Special 301” report
released by the Office of the U.S. Trade Representative.
Pharmaceutical Industry
In previous years, PhRMA has provided annual estimates of U.S. pharmaceutical industry losses
from foreign violations of data exclusivity and patent protection.23 In its 2007 Special 301
submission to the USTR, PhRMA contended that its member companies sustained damages
totaling an estimated $21.7 million from data exclusivity and patent violations in 24 countries
(see Table 2).24 Damages reported in the 2007 submission were nearly double those reported in
the prior year’s submission. While the total loss associated with IPR infringement grew, damages
23
PhRMA’s calculations of damage due to violations of data exclusivity are based on a five-year data protection
period; any sales not made by the patent holder within the data exclusivity period were regarded as data exclusivity
damages. For damages from patent protection violations, PhRMA used a ten-year patent protection period and
considered any sales not made by the patent holder within that period to be damages. For some countries, PhRMA did
not report damages because data was not available at the time.
24
Economic losses in PhRMA’s annual Special 301 submission are not reported on calendar-year basis because fourth
quarter economic data is not available at the time the report is issued.
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as a percentage of sales declined from the 2006 submission to the 2007 submission.25 At the time
of reporting for submissions for subsequent years, PhRMA was not able to provide estimates of
damages resulting from trade barriers associated with intellectual property protection and market
access.26
Table 2. Estimated Damages for PhRMA Member Companies From Data Exclusivity
and Patent Protection Violations
2006 Submission
(Oct. 2004 - Sept. 2005)
2007 Submission
(Oct. 2005 - Sept. 2006)
Total Damages
$13.9 million
$21.7 million
Total Sales
$74.6 million
$172.1 million
19%
13%
Damages as a Percentage of Sales
Source: PhRMA 2006 and 2007 Special 301 Submissions.
Limitations on Data Estimating IPR Infringement Costs
There may be limitations to data estimating the impact of counterfeiting and piracy on the U.S.
economy. According to a study conducted by the U.S. Government Accountability Office (GAO),
the U.S. government does not systematically collect data or analyze the impacts of counterfeiting
and piracy on the U.S. economy. In many cases, the federal government relies on estimates
conducted by industry groups. However, industry associations may not always release their
proprietary data sources and methods, complicating efforts to verify such estimates. 27 Some
critics point out that many of the estimates for losses associated with IPR infringement are
generated by industry groups that may have self-interested motivations.28
There is a possibility that such IPR infringement loss estimates may overestimate the extent to
which sales of pirated and counterfeit goods displace legitimate sales. Methods for calculating
data on counterfeiting and piracy often involve certain assumptions. Estimates of losses from IPR
infringement can be highly sensitive to how these assumptions are derived and weighted. Some
analysts question the proposition that sales of pirated goods translate directly into revenue losses
for legitimate firms. The basic economic model employed in such estimates assumes that there is
perfect substitutability between pirated and legitimate goods, which would equate sales of pirated
goods to revenue losses of legitimate U.S. copyright businesses. Some analysts suggest that
legitimate firms face a competition threat only if the individuals purchasing counterfeit products
would be able and willing to purchase the legitimate product at the price offered when piracy is
not present.29 For consumers in poor developing countries, especially, this assumption may not be
tenable. Others also question the statistical techniques used to develop these estimates. 30
25
26
PhRMA, Special 301 Submission for 2007. See Appendix: Damage Estimate Methodology, p. v.
PhRMA, Special 301 Submission 2008.
27
U.S. Government Accountability Office, Intellectual Property: Observations on Efforts to Quantify the Economic
Effects of Counterfeit and Pirated Goods, GAO-10-423, April 2010.
28
Monika Ermert, "Speculation Persists on ACTA as First Official Meeting Concludes," Intellectual Property Watch,
June 5, 2008. Robin Gross, IP Justice White Paper on the Proposed Anti-Counterfeiting Trade Agreement (ACTA), IP
Justice, March 25, 2008, p. 6.
29
Robert G. Picard, “A Note on Economic Losses Due to Theft, Infringement, and Piracy of Protected Works,” Journal
(continued...)
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At the same time, there is a possibility that some IPR infringement loss estimates may
underestimate the losses to U.S. businesses. For example, U.S. trade losses due to copyright
infringement may be higher than reported because estimates oftentimes do not account for all
forms of piracy, such as Internet piracy, which is an increasingly significant contributor to
copyright piracy.31 One study estimates that nearly 24% of global internet traffic infringes upon
copyright.32
The Organization Structure of IPR Protection
Given the importance of intellectual property to the U.S. economy and the economic losses
associated with counterfeiting and piracy, the United States is a leading advocate of strong global
IPR standards and enforcement. Increasingly, the United States has integrated IPR policy in its
international trade policy activities, pursuing enhanced IPR laws and enforcement through
multilateral, regional and bilateral trade agreements, and national trade laws.
Multilateral IPR System
World Trade Organization (WTO)
At the center of the present multilateral trading system is the World Trade Organization (WTO),
an international organization established in 1995 as the successor to the General Agreements on
Tariffs and Trade (GATT). The WTO was established as the result of the Uruguay Round of trade
negotiations (1986-1994), which resulted in numerous agreements on trade in goods, services,
investment and other non-tariff barriers to trade. One of the Uruguay Round agreements was the
Agreement on Trade-Related Aspects of Intellectual Property Rights (TRIPS Agreement), which
sets minimum standards on intellectual property rights protection and enforcement with which all
WTO member states must comply. The United States, the European countries, and the IPR
business community were instrumental in including IPR on the Uruguay Round agenda. Many
developing countries were wary of including IPR in trade negotiations, preferring to discuss them
under the World Intellectual Property Organization (WIPO) (see below) instead. However,
developing countries acceded, after being granted delayed compliance periods, and after
achieving negotiating goals on other issues such as textiles and clothing, and savoring the
prospect of operating under a rules-based trading system.
While previous international agreements on intellectual property rights continue to exist (see
Table 2), the TRIPS Agreement was the first time that intellectual property rules were
incorporated into the multilateral trading system. Two basic tenets of the TRIPS Agreement are
national treatment (signatories must treat parties of other WTO members no less favorably in
terms of IPR protection than the party’s own nationals) and most-favored-nation treatment (any
(...continued)
of Media Economics, 17(3), 207-217, 2004.
30
U.S. Government Accountability Office, Intellectual Property: Observations on Efforts to Quantify the Economic
Effects of Counterfeit and Pirated Goods, GAO-10-423, April 2010.
31
IIPA, “IIPA’s 2009 Special 301 Report on Copyright Protection and Enforcement,” submitted to the U.S. Trade
Representative by IIPA on February 17, 2009, http://www.iipa.com.
32
Envisional, Technical Report: An Estimate of Infringing Use of the Internet, January 2011.
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advantage in IPR protection granted to the party of another WTO member shall be granted to
nationals of all other WTO member states).
Much of the TRIPS Agreement sets out the extent of the agreement’s coverage of the various
types of intellectual property: copyrights, trademarks, geographical indications, industrial
designs, patents, layout of circuitry design, trade secrets, and test data. The TRIPS Agreement
provisions build on several existing IPR treaties administered by the WIPO (discussed below).
Another part provides standards of enforcement for IPR covered by the agreement. It enumerates
standards for civil and administrative procedures and remedies, the application of border
measures, and criminal procedures. A Council for the TRIPS Agreement was established to
monitor the implementation of the agreement and transition arrangements were devised for
developing countries. Finally, the agreement provides for the resolution of disputes under the
Uruguay Round Agreement’s Dispute Settlement Understanding (DSU). The binding nature of
the DSU, with the possibility of the withdrawal of trade concessions (usually the re-imposition of
tariffs) for non-compliance, sets this agreement apart from previous IPR treaties that did not have
effective dispute settlement mechanisms.
U.S. WTO Cases Against China on IPR
In April 2007, the United States filed two WTO dispute settlement cases against China, alleging inadequacies in
China’s enforcement of IPR laws and its barriers to market access for U.S. copyright businesses.33
•
In January 2009, the DSU issued its final ruling on the case centering on IPR enforcement issues. The WTO panel
ruled in the United States’ favor that China’s denial of copyright protection to works without censorship
approval is inconsistent with the TRIPS Agreement. The panel also agreed with the United States that it is
impermissible for China to publicly auction IPR-infringing goods seized at the border, with the only requirement
being that fake brands and trademarks be removed from the goods. The WTO panel ruled that more evidence
was needed before deciding whether or not China’s threshold values for prosecuting counterfeiting and piracy
permit commercial scale IPR infringement. China agreed to implement the WTO ruling. 34
•
In August 2009, a WTO panel ruled that a number of China’s restrictions on trading rights and distribution of
IPR-related products were inconsistent with WTO rules. However, the WTO panel did not address whether
China’s censorship policies or import limitations on foreign films violate WTO rules. China agreed to implement
the WTO ruling.35
The TRIPS Agreement also seeks a balance of rights and obligations between the private right,
enumerated above, and the obligation “to secure social and cultural development that benefits
all.”36 Article 7 declares that:
... the protection and enforcement of IPR should contribute to the promotion of technological
innovation and to the transfer and dissemination of technology, to the mutual advantage of
33
USTR, “United States Files WTO Cases Against China Over Deficiencies in China’s Intellectual Property Rights
Laws and Market Access Barriers to Copyright-Based Industries,” press release, April 9, 2007, http://www.ustr.gov.
See also CRS Report RL33536, China-U.S. Trade Issues, by Wayne M. Morrison.
34
WTO, “WTO issues panel report on U.S.-China dispute over intellectual property rights,” press release, January 26,
2009. USTR, “United States Wins WTO Dispute Over Deficiencies in China's Intellectual Property Rights Law,” press
release, January 26, 2009. Daniel Pruzin, "WTO Publishes Final Ruling in U.S. Complaint Against Chinese IPR
Enforcement Measures," International Trade Daily, January 27, 2009.
35
For more information on U.S-China IPR and other trade issues, see CRS Report RL33536, China-U.S. Trade Issues,
by Wayne M. Morrison.
36
Pascal Lamy, “Trade-Related Aspects of Intellectual Property Rights - Ten Years Later,” Journal of World Trade,
October 2004, p. 925.
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producers and users of technological knowledge and in a manner conducive to social and
economic welfare and to a balance of rights and obligations.
This paragraph attempts to link the protection of IPR with greater technology transfer, including
technology covered by IPR protection, to the developing world. The language itself has been
interpreted in various ways. Developed countries have tended to consider this language
exhortatory, but developing countries have tried, without much success, to make technology
transfer a meaningful obligation within the TRIPS Agreement system. Article 66.2 of the
agreement requires developed country members to provide incentives to their enterprises and
institutions to promote technology transfer to least-developed countries to assist them in
establishing a viable technology base. Developed countries report annually on their efforts to
encourage technology transfer (LDCs).
Complying with international IPR standards may impose greater burdens on developing countries
than developed countries. Developing countries generally have to engage in greater efforts to
bring their laws, judicial processes, and enforcement mechanism into compliance with the TRIPS
Agreement. Consequently, developing countries were given an extended period of time in which
to bring their laws and enforcement mechanisms into compliance with the TRIPS Agreement.
Developing countries and post-Soviet states were given an additional four years from the entry
into force of the agreement (January 1, 1995). For products that were not covered by a country’s
patent system (such as pharmaceuticals in many cases), an additional five years was granted to
bring such products under coverage. For developing countries, all provisions of the TRIPS
agreement should now be in force. For the least developed countries (LDCs), the phase-in period
was set at 10 years (January 1, 2006), and for pharmaceuticals, the compliance period was later
extended to 2016.37
Declaration on TRIPS Agreement and Public Health 38
In agreeing to launch the Doha Round of WTO trade negotiations, trade ministers adopted a
“Declaration on the TRIPS Agreement and Public Health” on November 14, 2001.39 The
Declaration sought to alleviate developing country dissatisfaction with aspects of the TRIPS
regime. It delayed the implementation of patent system provisions for pharmaceutical products
for least developed countries (LDCs) until 2016. The declaration committed member states to
interpret and implement the agreement to support public health and to promote access to
medicines for all. The Declaration recognized certain “flexibilities” in the TRIPS agreement to
allow each member to grant compulsory licenses for pharmaceuticals and to determine what
constitutes a national emergency, expressly including public health emergencies such as
HIV/AIDS, malaria, and tuberculosis or other epidemics.
Paragraph 6 of the Declaration directed the WTO members to formulate a solution to a corollary
concern, the use of compulsory licensing by countries with insufficient or inadequate
manufacturing capability. Compulsory licenses are issued by governments to authorize the use or
37
“Extension of the Transition Period under Article 66.1 of the TRIPS Agreement for Least-Developed Country
Members for Certain Obligations with Respect to Pharmaceutical Products,” WTO Document IP/C/25, July 1, 2002.
38
See CRS Report R40607, Intellectual Property Rights and Access to Medicines: International Trade Issues, by
Shayerah Ilias.
39
Declaration on the TRIPS Agreement and Public Health, (WT/MIN(01)/DEC/2), November 14, 2001, available at
http://www.wto.org/english/thewto_e/minist_e/min01_e/mindecl_trips_e.htm.
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production of a patented item by a domestic party other than a patent holder. They are authorized
by Article 31 of TRIPS, which places certain limitations on their use, scope, duration. A provision
that predominantly restricted production authorized by compulsory license to the domestic market
became the focal point of the negotiations because it, in effect, conveys the right of compulsory
licensing only to countries with the capability to manufacture a given product. Countries without
a domestic manufacturing capability were essentially precluded from using this flexibility of the
TRIPS agreement.
On the eve of the Cancun Ministerial in August 2003, WTO members agreed on a Decision40 to
waive the domestic market provision of the TRIPS article on compulsory licensing (Article 31(f))
for exports of pharmaceutical products for “HIV/AIDS, malaria, tuberculosis and other
epidemics” to least developed countries (LDCs) and countries with insufficient manufacturing
capacity. This Decision was incorporated as an amendment to the TRIPS agreement at the Hong
Kong Ministerial in December 2005.
The amendment must be ratified by two-thirds of the 153 WTO member states. The deadline for
ratification has been extended to December 30, 2011. Until then, the 2003 waiver continues in
force. To date, the following WTO members have ratified the amendment: the United States,
Switzerland, El Salvador, South Korea, Norway, India, the Philippines, Israel, Japan, Australia,
Singapore, Hong Kong, China, the 27 countries of the European Union, Mauritius, Egypt,
Mexico, Jordan, Brazil, Morocco, Albania, Macau, Canada, Bahrain, Colombia, Zambia,
Nicaragua, Pakistan, the Former Yugoslav Republic of Macedonia, Uganda, Mongolia, Croatia,
and Senegal.41
The system established by the WTO allows LDC and countries without sufficient manufacturing
capacity to issue a compulsory license to a company in a country that can produce such a product.
After a matching compulsory license is issued by the producer country, the drug can be
manufacturing and exported subject to various notification requirements, quantity and safeguard
restrictions. While several exporting countries have established laws and procedures for
implementing this system, only Rwanda has availed itself to use the system to import HIV/AIDS
medicines from a generic manufacturer in Canada.42
40
“Implementation of Paragraph 6 of the Doha Declaration on the TRIPS Agreement and Public Health,” IP/C/W/405,
August 30, 2003, and accompanying Chairman’s statement, available at http://www.wto.org/english/news_e/pres03_e/
pr350_e.htm.
41
“Members accepting amendment of the TRIPS Agreement,” http://www.wto.org/english/tratop_e/trips_e/
amendment_e.htm.
42
“Canada Issues Compulsory License For HIV/AIDS Drug Export To Rwanda, In First Test Of WTO Procedure,”
Bridges Weekly Trade News Digest, September 26, 2007, http://www.ictsd.org/weekly/07-09-26/story2.htm.
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Intellectual Property Protection and Development
The controversy over the relationship between IPR and development was engaged by the advent of the TRIPS
Agreement, which for the first time placed IPR obligations on developing countries. Some hold that expansion of IPR
is an obstacle to growth and development in less advanced countries, while others, with a diametrically opposing
view, maintain that IPR are beneficial to both developed and developing countries.
Some IPR critics believe that a strong IPR regime may reduce developing countries’ access to technology from
advanced countries by imposing higher fees for technology licenses and production right, limiting their innovation and
economic growth and development. For instance, Japan, Singapore, Taiwan, and South Korea enhanced their
technological abilities and developed their economies through “reverse engineering” of foreign technologies.
Others claim that IPR promote technology transfer through increased trade, foreign investment, and licensing in the
long-run by making a country more attractive to foreign partners. A 2002 OECD study concluded that stronger IPR
laws, particularly enhanced patent standards, may be associated with increased foreign direct investment (FDI) and
trade for developing countries over time, with variation by industries and level of development.43 For instance, India
experienced an increase in foreign investment and technology transfer once it expanded its patent protection. China
offers a counterexample of a country with a weak IPR regime but high FDI and trade levels.
There is also evidence that IPR’s impact on developing countries may vary by the level of development. One study
suggests that IPR protection may offer more benefits for the more industrialized developing countries, such as Brazil
and India, compared to other developing countries. Such industrializing economies could experience economic
growth of as much as 0.5% annually through increased trade, FDI, and licensing.44 Another study finds that rapid
economic growth is associated with weak intellectual property regimes, but that developing countries with higher
levels of per capita income may benefit economically from stronger IPR regimes.45
There is also concern that strengthened patent protection may drive up prices for medicines or delay the entry of
generic drugs into the market, reducing access to HIV/AIDS treatments and other drugs. IPR supporters argue that
strong IPR is critical to creating incentives for pharmaceutical innovations and suggest that reduced prices are no
guarantee that needed goods will make it into the hands of individuals in developing countries due to political
corruption, poverty, and poor social infrastructure.
World Intellectual Property Organization (WIPO)
In addition to the WTO, the other main multilateral venue for addressing IPR issues is the World
Intellectual Property Organization (WIPO), a United Nations agency. Established in 1967, WIPO
is charged with fostering the effective use and protection of intellectual property globally. WIPO’s
mandate focuses exclusively on intellectual property, in contrast to the WTO’s broader
international trade mandate. WIPO’s antecedents are the 1883 Paris Convention for the Protection
of Industry Property and the 1886 Berne Convention for the Protection of Literary and Artistic
Work. Most of the substantive provisions of these two treaties are incorporated in the WTO’s
TRIPS Agreement. WIPO’s primary function is to administer a group of IPR treaties which put
forth minimum standards for member states (shown in Table 3). All international IPR treaties,
save TRIPS, are administered by WIPO.
In order to address digital technology issues not dealt with in the TRIPS Agreement, WIPO
established the WIPO Copyright Treaty (WCT) and WIPO Performance and Phonograms Treaty
(WPPT) in 1996.46 Recent WIPO efforts have focused on patent law. In June 2000, WIPO
43
OECD, The Impact of Trade-Related Intellectual Property Rights on Trade and Foreign Direct Investment in
Developing Countries, May 28, 2003, p. 21, http://www.oecd.org.
44
Keith E. Maskus, Intellectual Property Rights in the Global Economy, Institute for International Economics (IIE),
Washington, D.C., August 2000.
45
Commission on Intellectual Property Rights (CIPR), Integrating Intellectual Property Rights and Development
Policy, September 2002.
46
These WCT and WPPT frequently are referred to as the WIPO Internet Treaties.
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signatories adopted the Patent Law Treaty (PLT), which called for harmonization of patent
procedures. This agreement went into force on April 28, 2005. Discussions began in May 2001
for the Substantive Patent Law Treaty (SPLT), which targets issues specifically related to patent
grants, but stalled in 2006. Government leaders participating in the Group of 8 (G8) meeting in
July 2008 called for “accelerated discussions” of the SPLT.47
WIPO’s other functions include assisting member states through training programs, legislative
information, intellectual property institutional development, automation and office modernization
efforts, and public awareness activities. WIPO’s enforcement activities are more limited than
those of the WTO. Through its Advisory Committee on Enforcement (ACE), WIPO cooperates
with member states to promote international coordination on enforcement activities.
With the emergence of the TRIPS Agreement, some observers question the relevance of WIPO.
However, others contend that the TRIPS Agreement has given WIPO a new and stronger role.
Through a 1996 agreement between the WTO and WIPO, the two organizations have agreed to
work closely together to ensure the implementation of the TRIPS Agreement by member states
through legal and technical assistance and technical cooperation. 48 In 1998, WIPO and WTO
began a joint initiative based on the 1996 agreement to enhance their coordination of technical
cooperation activities in order to assist developing countries, in particular, to fulfill their TRIPS
commitments.49
Table 3. Summary of WIPO-Administered IPR Treaties
Treaty
Date
Concluded
Provisions
Intellectual Property Protection Treaties
Paris Convention for the Protection of Industrial
Property (Paris Convention)
1883
(entered
into force
1884)
Protects industrial property (includes patents,
marks, industrial designs, utility models, trade
names, and geographic indications)
Berne Convention for the Protection of Literary
and Artistic Works (Berne Convention)
1886
(entered
into force
1886)
Protects literary and artistic works, providing
right to control and receive payments for use
Madrid Agreement for the Repression of False
and Deceptive Indications of Source on Goods
(Madrid Agreement - Indications of Source)
1891
Requires States to seize imported goods with
false/deceptive indications of source or to
prohibit importation of such goods; open to
States party to Paris Convention (1883)
Rome Convention for the Protection of
Performers, Producers of Phonograms and
Broadcasting Organizations (Rome Convention)
1961
Protects rights of performers against certain acts
to which they have not agreed; protects rights of
producers of phonograms, and broadcasting
organizations to authorize/prohibit certain acts;
open to States party to Berne Convention (1886)
Convention for the Protection of Producers of
1971
Protects producers of phonograms against
47
Monika Ermert, "G8 Governments Want ACTA Finalised This Year, SPLT Talks Accelerated ," Intellectual
Property Watch, July 9, 2008.
48
“Agreement between the World Intellectual Property Organization and the World Trade Organization,”
http://www.wto.org/english/tratop_e/trips_e/wtowip_e.htm.
49
WIPO, Intellectual Property Handbook, http://www.wipo.org, p. 359.
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Treaty
Date
Concluded
Phonograms Against Unauthorized Duplication of
their Phonograms (Phonograms Convention)
Provisions
unauthorized reproduction of their phonograms
or importation of duplications for public
distribution
Brussels Convention Relating to the Distribution
of Programme-Carrying Signals Transmitted by
Satellite (Brussels Convention)
1974
Protects against the unauthorized distribution of
program-carrying signals transmitted by satellite
Nairobi Treaty on the Protection of the Olympic
Symbol (Nairobi Treaty)
1981
Protects Olympic symbol against unauthorized
commercial uses
Treaty on the International Registration of
Audiovisual Works (Film Register Treaty)
1989
Establishes International Register for Audiovisual
Works
Treaty on Intellectual Property in Respect to
Integrated Circuits (Washington Treaty)
1989
Protects layout designs which display electrical
components of an integrated circuit
Trademark Law Treaty (TLT)
1994
Streamlines national and regional trademark
registration processes
WIPO Copyright Treaty (WCT)
1996
(entered
into force
2002)
Special agreement under Berne Convention;
grants exclusive rights to owners of copyright in
computer programs and compilations of
data/other material
WIPO Performances and Phonograms Treaty
(WPPT)
1996
(entered
into force
2002)
Grants exclusive rights to performers and
phonogram producers
Patent Law Treaty (PLT)
2000
(entered
into 2005)
Aims to harmonize and streamline national and
regional patent application procedures and
patents
Singapore Treaty on the Law of the Trademarks
2006 (not
yet in force)
Builds on TLT (1994); aims to harmonize
trademark registration procedures; has wider
scope (includes communication technology
developments)
Budapest Treaty on the International Recognition
of the Deposit of Microorganisms for the
Purposes of Patent Procedure (Budapest Treaty)
1977
(entered
into force
1980)
Special agreement under Paris Convention (1883);
requires States to recognize the deposit of a
microorganism with any “international depositary
authority”
Madrid Agreement Concerning the International
Registration of Marks (Madrid Agreement Marks)
1891
Requires seizure of imported goods with
false/deceptive indication of source or prohibition
of importation of such goods; open to States
party to Paris Convention (1883)
Hague Agreement Concerning the International
Registration of Industrial Designs (Hague
Agreement)
1925
(entered
into force
1928)
Allows protection of industrial designs in all
member states on basis of single application with
WIPO; three acts currently in force: 1934, 1960,
and 1999 Acts
Lisbon Agreement for the Protection of
Appellations of Origin and their International
Registration (Lisbon Agreement)
1958
Provides international protection for geographical
indications
Patent Cooperation Treaty (PCT)
1970
(entered
into force
1978)
Establishes an international patent filing system;
allows a single international patent application to
have legal standing in all countries signatory to
PCT; open to States party to Paris Convention
Global Protection System Treaties
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Treaty
Date
Concluded
Provisions
(1883)
Protocol Relating to the Madrid Agreement
(Madrid Protocol )
1989
(entered
into force
1995)
Relates to Madrid Agreement (1891); seeks to
make Madrid system more amenable to domestic
laws of certain who are not yet signatories to
Madrid Agreement; open to States party to Paris
Convention (1883)
Nice Agreement Concerning the International
Classification of Goods and Services of the
Purposes of the Registration of Marks (Nice
Agreement)
1957
(entered
into force
1961)
Establishes a classification of goods and services in
order to register trademarks and service marks;
open to States party to Paris Convention (1883)
Locarno Agreement Establishing an International
Classification for Industrial Designs
1968
(entered
into force
1971)
Establishes a classification for industrial designs;
open to States party to Paris Convention (1883)
Strasbourg Agreement Concerning the Industrial
Patent Classification (Strasbourg Agreement)
1971
(entered
into force
1975)
Establishes the International Patent Classification
(IPC); open to States party to Paris Convention
(1883)
Vienna Agreement Establishing Classification of
the Figurative Elements of Marks (Vienna
Agreement)
1973
(entered
into force
1985)
Establishes a classification for marks which
consist/contain figurative components; open to
States party to Paris Convention (1883)
Classification Treaties
Source: WIPO.
Free Trade Agreements
In recent years, the United States increasingly has focused on free trade agreements (FTAs) as an
instrument to promote stronger IPR regimes by foreign trading partners. In general, the United
States has viewed the TRIPS Agreement and WIPO-administered treaties as a minimum standard
and has pursued higher IPR protection and enforcement levels through regional and bilateral
agreements.
Trade Promotion Authority and Negotiating Objectives
Under Trade Promotion Authority (TPA), Congress delegates its constitutional authority to
regulate foreign commerce to the President to negotiate and enter into certain free trade
agreements (FTAs), and to have their implementing bills considered under expedited legislative
procedures (no amendment, up-or-down vote), provided the President follows the guidelines,
objectives, reporting, and consultation requirements mandated by Congress. IPR have become
important negotiating objectives in grants of trade promotion authority; the most recent extension
of that authority expired on July 1, 2007.
IPR negotiating objectives for FTAs were first enacted in trade promotion authority (then known
as fast-track authority) by the Omnibus Trade and Competitiveness Act of 1988 (P.L. 100-418).
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The act sought enactment and enforcement of adequate IPR protection from negotiating partners.
It also sought to strengthen international rules, dispute settlement, and enforcement procedures
through the GATT and other existing intellectual property conventions. This negotiating mandate
led to the establishment of the TRIPS Agreement during the Uruguay Round and the IPR
provisions in the North American Free Trade Agreement (NAFTA). In the intervening period
since the 1988 Act, the TRIPS agreement came into force and the IPR provisions of NAFTA
became the template for future bilateral or regional FTAs. Thus, the focus of IPR negotiating
objectives shifted from creating to strengthening the IPR trade regime.
More recent FTA negotiations have been conducted under the Trade Promotion Authority Act of
2002 (P.L. 107-210), which included two broad IPR negotiating objectives. One broad objective
was to apply the existing IPR protection to digital media. The negotiating objectives contained
provisions to extend IPR protection to new and emerging technologies and to methods of
transmission and dissemination. The language called for standards of enforcement to keep pace
with technological change and to allow rights-holders the legal and technological protections for
their works over the Internet and other new media.
A second broad objective of the Trade Promotion Authority Act of 2002 was to negotiate trade
agreements in terms of IPR that “reflect a standard of protection similar to that found in U.S.
law.”50 This phrase opened the door to the negotiation of provisions that go beyond the level of
protection provided in the TRIPS agreement. Often referred to as “TRIPS-plus” provisions, these
obligations include expanding coverage to new sectors; establishing more extensive standards of
protection; and reducing the flexibility options available in TRIPS. Some of the new measures
also address technological innovations that have come about since the TRIPS Agreement.
In May 2007, the Bush Administration and Congress concluded a bipartisan agreement on trade
policy that addressed some Members’ concerns about the implications of enhanced IPR on
developing countries’ ability to meet public health needs.51 In particular, congressional leadership
sought to ensure that pending FTAs allowed trading partners to have enough flexibility to meet
their IPR obligations and to be able to promote access to life-saving medicines, while otherwise
meeting their international IPR protection and enforcement obligations. IPR language previously
negotiated in the FTAs with the developing countries of Peru, Panama, and Colombia
subsequently were modified to reflect the agreement. Because Korea is an industrialized country,
the United States did not significantly scale-down the patent protection obligations in the U.S.Korea FTA.
Current IPR-Related U.S. FTA Activity
In 2011, the Obama Administration may ask Congress to approve a free trade agreement (FTA)
with South Korea, as well as FTAs with Colombia and Panama. These three FTAs were
negotiated by the Bush Administration, but have not been implemented.
Meanwhile, the Obama Administration has entered into negotiations with participants in the
Trans-Pacific Partnership (TPP) Agreement—Australia, Brunei, Chile, New Zealand, Peru,
Malaysia, Singapore, and Vietnam. The objective is to build on U.S. trade ties in the region
50
P.L. 107-210, Sec. 2102(b)(4).
The May 10, 2007 bipartisan trade agreement is available online at:
http://www.ustr.gov/assets/Document_Library/Fact_Sheets/2007/asset_upload_file127_11319.pdf.
51
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already established in FTAs with Australia, Chile, and Singapore and to provide a high-standard
framework for expanded free trade in the region.20 IPR, particularly in the area of
pharmaceuticals, may prove to be a contentious issue in the negotiation of the TPP.
In addition, the Obama Administration has been conducting negotiations on the AntiCounterfeiting Trade Agreement (ACTA), a proposed agreement being negotiated by Australia,
Canada, the 27 member states of the European Union, Japan, South Korea, Mexico, Morocco,
New Zealand, Singapore, Switzerland, and the United States. Negotiations on the ACTA
Agreement began under the Bush Administration. The ACTA would build on the minimum
standards for IPR protection and enforcement set forth by the TRIPS Agreement. It is being
crafted independent of any existing international organization or agreement. The eleventh and
final round of negotiations concluded on October 2, 2010, and the ACTA participants released to
the public a draft text of the agreement. ACTA participants are working to resolve outstanding
issues in the agreement. 52
Central IPR Standards in U.S. FTAs
What follows is a discussion of some of the central patent and copyright standards sought in
FTAs that are currently in force or have been signed by the United States (see Table 4).53
Patents
Patent protection is arguably the most contentious area of U.S. FTA negotiations on IPR issues.
While the United States and other developed countries advocate for strong patent protections in
order to promote innovation, there is concern that such stringent protections may delay
developing countries’ access to generic drugs and increase prices. Many of the FTAs in force
include TRIPS-plus patent provisions, the most prominent of which are patent term length
extensions, linkages between regulatory authority and patent status, data protection, compulsory
licensing and parallel importation. The FTAs with Peru, Panama, and Colombia respond to the
concerns of some Members of Congress over provisions that could restrict access to medicines in
these countries and contain less ambitious standards for pharmaceutical patents, compared to
previously negotiated FTAs. Pharmaceutical industry advocates express concern that this scaledown in patent protection in these FTAs may set a precedent for future FTA negotiations. 54
Patent Term Extensions: Many FTAs include provisions for mandatory patent term length
extensions beyond the TRIPS Agreement obligation of patent protection terms of twenty years
from the filing date. These FTAs allow for extensions in cases of “unreasonable” delays in the
issuance of patents due to the regulatory review or administrative process. Patent holders contend
that such measures enhance the ability of rights-holders to recoup the costs of research and
development of new products. However, there is concern that patent terms extensions may delay
the entry of generic drugs into a market. In a scale-down from TRIPS-plus obligations, FTAs with
52
For more information, see CRS Report R41107, The Proposed Anti-Counterfeiting Trade Agreement: Background
and Key Issues, by Shayerah Ilias.
53
For a more detailed discussion of the differences between the TRIPS Agreement and regional FTAs that are in force,
see CRS Report RL33205, Intellectual Property and the Free Trade Agreements: Innovation Policy Issues, by John R.
Thomas.
54
"Brand-Name Industry Alarmed at IPR Precedent of FTA Template," Inside US Trade, May 18, 2007.
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Peru, Colombia, and Panama state that patent term restorations for pharmaceutical products are
optional.
Patent Linkages: In general, the term “patent linkage” refers to the attachment of regulatory
approval for the marketing of a drug with the status of a patent. If a patent exists, the FDA and its
counterparts in other countries may not grant marketing approval for a generic version of a drug
that is patented in the country without the permission of the patent holder. Patent linkage is a
common provision in the trade agreements obtained by the United States. This presents a
departure from TRIPS, under which generic drug manufacturers are able to apply for marketing
approval without the patent owner’s permission and prior to the expiration of the patent; this may
reduce the time it takes for generic drugs to enter a market once the patent expires.55 In light of
developing country concerns about delays in access to generic versions of drugs, FTAs signed
with Peru, Panama, and Colombia do not tie marketing approval for a generic drug with the
patent status of its brand name drug.
Data Protection: In cases where the patent holders must submit undisclosed data regarding the
safety or effectiveness of new pharmaceutical or agricultural products in order to market them,
the TRIPS Agreement requires members to take measures to protect such data from disclosure
and unfair commercial use. The TRIPS agreement does not prescribe any time period for this
protection. Recent U.S. FTAs take these standards a step further, generally requiring a five-year
period of marketing exclusivity for the patent holder, which typically begins from the date the
product is approved in the country. Under this TRIPS-plus provision, generic drug manufacturers
who want to market and distribute a generic version of a drug while the data exclusivity period is
in effect must conduct their own clinical trials and submit their own findings to the national drug
regulatory authority; they cannot rely on the findings submitted by the patent holder. Some critics
contend that such provisions may raise the cost of manufacturing generic versions of patented
drugs, as well as delay access to generic forms of drugs. The FTAs with Peru, Panama, and
Colombia now include provisions that may reduce data exclusivity terms of five years by a
minimum of six months in practice.56
Compulsory Licensing: A compulsory license is an authorization by a government for third
parties (such as a company or the government itself) for the manufacture or use of a product
under patent without the permission of the rights- holder. The TRIPS Agreement permits
signatories to issue compulsory licenses for patented devices and provide compensation to the
owner of the patent and does not limit the situations in which such licenses may be issued. The
third party must have attempted to obtain permission from the patent holder, although this
requirement is waived in times of national emergency or other extenuating circumstances. U.S.
FTAs with Australia and Singapore limit attaining compulsory licenses only for domestic use and
to situations of remedying antitrust violations or in situations of public non-commercial use,
national emergency, or other cases of extreme need. Also under these FTAs, the patent holder is
under no obligation to provide test data, technical know-how or other undisclosed information for
the patent subject to compulsory license. The compulsory license provisions have not been
included in FTAs with developing countries.
55
While TRIPS does not directly speak to the rights of generic drug manufacturers in obtaining marketing approval for
a generic drug before the expiration of the patented drug, Article 30 of TRIPS permits exceptions of patent rights for
activities such as “research, prior user rights, and pre-expiration testing.”
56
For example, under the Peru FTA, if a company files to market a new drug in Peru after making an initial filing in
another country, such as the United States, and Peru approves the drug within six months of the filing, the data
exclusivity period begins at the time the drug was approved in the country of the initial filing, not Peru.
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Parallel Importation: Parallel imports, also known as grey-market goods, refer to goods
imported into a country without permission of the rights-holder after those goods were
legitimately sold elsewhere. Parallel importation relates to the concept of territorial exhaustion of
IPR, which governs the extent of IPR after the first sale. Under a national system of exhaustion
practiced in the United States, IPR are exhausted domestically after the first sale, but not abroad,
thus prohibiting trade in those goods without permission of the rights-holder. Under an
international system, IPR are exhausted at the first sale for any destination, and such goods can be
exported freely. Article 6 of the TRIPS specifically excludes issues arising from exhaustion of
IPR from WTO dispute settlement, allowing each member to adopt different exhaustion regimes.
Thus, TRIPS does not address the issue of parallel imports. Some developing countries contend
that parallel importation is an alternative method for governments to increase access to medicines
in the absence of a compulsory license. 57 Pharmaceutical companies have voiced concerns that
this practice threatens their ability to engage in price differentiation between different markets.
U.S. FTAs negotiated with Australia, Singapore, and Morocco disallow parallel importing of
patented products. Subsequent U.S. negotiated FTAs have not included this provision, due to
language included in the Science, State, Justice, and Commerce, and Related Agencies,
Appropriations Act of 2006 (P.L. 109-108), which prohibited the use of such provisions.
. They may take forms such as patents, trade
secrets, copyrights, trademarks, or geographical indications. Congress has constitutional
responsibility for legislating and overseeing IPR and international trade policy. Responsibility for
developing IPR policy, engaging in IPR-related international negotiations, and enforcing IPR
laws cuts across multiple U.S. government agencies.
The protection and enforcement of IPR is an important and longstanding component of U.S.
international trade policy and U.S. trade negotiating objectives. U.S. trade policy also seeks to
address new and evolving issues in the IPR landscape related to the growing role of emerging
markets in the global market place and the increased level of digital trade.
Since the North American Free Trade Agreement (NAFTA) and the 1995 Agreement on TradeRelated Aspects of Intellectual Property Rights (TRIPS Agreement) at the World Trade
Organization (WTO), trade policy has been used to advance IPR rules internationally. The TRIPS
Agreement set minimum standards for IPR protection and enforcement. The United States
engages in efforts with other trading partners to build on the TRIPS Agreement, particularly
through the negotiation of regional and bilateral free trade agreements (FTAs). To date, the United
States has entered into 14 FTAs with 20 countries, which generally include IPR commitments
exceeding obligations under the TRIPS Agreement. The May 10, 2007, bipartisan trade
agreement modified some of the IPR requirements in the U.S. FTAs with Peru, Panama and
Colombia, allowing for greater flexibility for these developing countries to meet both their IPR
obligations and public health needs. IPR issues are prominent in the ongoing U.S. FTA
negotiations of the proposed Trans-Pacific Partnership (TPP) and Transatlantic Trade and
Investment Partnership (TTIP). The United States also seeks to build on the TRIPS Agreement in
other ways, such as through the negotiation of the Anti-Counterfeiting Trade Agreement (ACTA).
Other trade policy tools also are available to advance U.S. international IPR objectives. Pursuant
to Section 182 of the Trade Act of 1974 as amended (P.L. 93-618), the Office of the U.S. Trade
Representative (USTR) identifies countries providing inadequate IPR protection in its annual
“Special 301” report. Section 337 of the amended Tariff Act of 1930 authorizes the U.S.
International Trade Commission (ITC) to prohibit U.S. imports that infringe on U.S. IPR.
Additionally, under the Generalized System of Preferences (GSP), the United States may consider
a developing country’s IPR policies and practices as a basis for offering or suspending
preferential duty-free entry to certain products from the country.
IPR issues related to international trade policy may figure prominently in the 113th congressional
agenda. Congress may:
•
examine the role of IPR in U.S. trade policy, including through consideration of
IPR trade negotiating objectives in a renewal of Trade Promotion Authority
(TPA);
•
conduct oversight of implementation of the IPR commitments in existing trade
agreements, as well as in the current U.S. trade negotiations on the TPP and
TTIP;
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•
conduct oversight of the role of IPR in U.S. economic growth and innovation,
and how the protection and enforcement of IPR relates to other public policy
goals, such as access to medicines in poor or developing countries and the free
flow of data;
•
consider the possibility of additional policy options to address IPR concerns in
emerging economies that are not a part of existing U.S. FTAs or included in
current U.S. FTA negotiations, as well as new and evolving IPR issues, such as
with respect to indigenous innovation, “forced” localization barriers to trade, and
trade secret theft through cybercrime; and
•
examine the effectiveness of the current U.S. coordinating structure and the
adequacy of current federal resources for promoting international IPR support.
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Contents
Introduction...................................................................................................................................... 1
Intellectual Property Rights Basics .................................................................................................. 1
Types of IPR .............................................................................................................................. 1
Patents ................................................................................................................................. 2
Trade Secrets ....................................................................................................................... 2
Copyright............................................................................................................................. 2
Trademarks .......................................................................................................................... 3
Infringement of IPR ................................................................................................................... 3
Piracy................................................................................................................................... 4
Counterfeiting ..................................................................................................................... 4
Innovation Indicators ....................................................................................................................... 4
Role of Intellectual Property in U.S. Economy ............................................................................... 6
Prevalence and Economic Consequences of IPR Infringement ....................................................... 8
Limitations on Data Estimating IPR Infringement Costs .......................................................... 8
International Economic Effects of IPR Infringement .............................................................. 10
U.S. Economic Effects of IPR Infringement ........................................................................... 11
Customs Seizure Data ....................................................................................................... 11
Economic Loss Estimates.................................................................................................. 12
The Organizational Structure of IPR Protection ............................................................................ 13
Multilateral IPR System .......................................................................................................... 13
World Trade Organization (WTO) .................................................................................... 13
Declaration on TRIPS Agreement and Public Health ....................................................... 15
World Intellectual Property Organization (WIPO) ............................................................ 17
Free Trade Agreements ............................................................................................................ 18
Trade Promotion Authority and Negotiating Objectives ................................................... 18
IPR in Current Trade Negotiations .................................................................................... 20
Central IPR Standards in U.S. FTAs ................................................................................. 22
U.S. Trade Law .............................................................................................................................. 29
Special 301 .............................................................................................................................. 29
Section 337 .............................................................................................................................. 31
Generalized System of Preferences ......................................................................................... 32
Issues for Congress ........................................................................................................................ 33
U.S. Efforts to Promote IPR Through Trade Policy ................................................................ 33
Addressing IPR Trade Challenges in Emerging Economies ................................................... 33
Effectiveness of the U.S. IPR Organizational Structure .......................................................... 35
Looking Forward ........................................................................................................................... 36
Figures
Figure 1. Composition of U.S. Border Seizures of Counterfeit and Pirated Goods,
FY2012 ....................................................................................................................................... 11
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Tables
Table 1. Global Intellectual Property Filings Through the PCT, 2010-2012 ................................... 5
Table 2. Estimated International Economic Losses Due to Counterfeiting and Piracy,
Selected Years ............................................................................................................................. 10
Table 3. Estimated U.S. Economic Losses Due to Counterfeiting and Piracy............................... 12
Table 4. USTR 2013 Special 301 Report: Country Designations .................................................. 31
Appendixes
Appendix A. Summary of WIPO Treaties ..................................................................................... 37
Appendix B. Patent and Copyright Provisions in the TRIPS Agreement and U.S. FTAs ............. 39
Appendix C. Overview of IPR-Related U.S. Government Agencies and Coordinating
Bodies ......................................................................................................................................... 42
Contacts
Author Contact Information........................................................................................................... 47
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Introduction
Intellectual property rights (IPR) traditionally have been matters of national concern. Individual
nation states have developed IPR regimes reflecting their domestic needs and priorities. Over
time, intellectual property protection and enforcement have come to the forefront as a key
international trade issue for the United States—largely due to the importance of intellectual
property as an prominent feature of an innovative U.S. economy—figuring prominently in the
multilateral trade policy arena and in regional and bilateral U.S. free trade agreements (FTAs).
Congress has legislative, oversight, and appropriations responsibilities related to IPR and trade
policy. The role of Congress in addressing IPR and trade-related issues stems from the U.S.
Constitution, which provides Congress with the power “To promote the Progress of Science and
useful Arts, by securing for limited Times to Authors and Inventors the exclusive Right to their
respective Writings and Discoveries” and “To regulate Commerce with foreign Nations.”1
Congressional interest has grown in the role of IPR in advancing U.S. industrial competitiveness
and contributing to U.S. economic recovery following the recent international financial crisis.
Some Members of Congress also have expressed concern about U.S. economic losses associated
with IPR infringement; the potential health and safety consequences of counterfeit
pharmaceutical drugs and other products; the national security implications of the theft of trade
secrets, including through cybercrime; and connections between organized crime and IPR
infringement.
This report discusses the different kinds of IPR and forms of IPR infringement; the role of IPR in
the U.S. economy; estimated losses associated with IPR infringement; the organizational structure
of IPR protection in multilateral, regional, bilateral arenas; U.S. government agencies involved
with IPR and trade; and issues for Congress regarding IPR and international trade.
Intellectual Property Rights Basics
This section provides definitions of various kinds of intellectual property rights (patents, trade
secrets, copyrights, trademarks, and geographical indications) and intellectual property rights
misappropriation (infringement, piracy, and counterfeiting).
Types of IPR
IPR are legal rights granted by governments to encourage innovation and creative output. They
ensure that creators reap the benefits of their inventions or works and may take forms such as
patents, trade secrets, copyrights, trademarks, or geographical indications. Through IPR,
governments grant a temporary legal monopoly to innovators by giving them the right to limit or
control the use of their creations by others. IPR may be traded or licensed to others, usually in
return for fees and/or royalty payments. Although the World Trade Organization (WTO)
Agreement on Trade-Related Aspects of Intellectual Property Rights (TRIPS) provides minimum
standards for IPR protections, such rights are granted on a national basis and are, in general,
enforceable only in the country in which they are granted. However, countries are obliged to
1
U.S. Constitution, Article 1, Section 8.
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abide by WTO rules, and their IPR enforcement practices can be challenged by other countries at
the WTO.
Patents
The Patent Act (35 U.S.C. 101 et seq.) governs the issuance and use of patents in the United
States. Patents are granted for inventions of new products, processes, or organisms (known as
utility patents). Patents also may be granted for designs and plants. For an invention to be
patentable, it must be new, “non-obvious” (involving an inventive step), and have a potential
industrial or commercial application. The patent provides the holder with the exclusive right to
exclude others from making, using, selling, or importing into the United States the patented
invention for a period of 20 years2 The patent right is based on the proposition that inventors must
be granted a temporary monopoly over their invention in order to encourage innovation and to
promote the expenditure of money on research and development (R&D). The patent holder
recoups these up-front costs through a temporary monopoly over the invention. In return for this
economic rent, the patent holder must disclose the content of the patent along with test data and
other information concerning the invention. This is meant to spur further creativity by those
seeking to build on the patent after its expiration. Domestically, patents are granted by the U.S.
Patent and Trademark Office (PTO) of the Department of Commerce.
Trade Secrets
A trade secret is any type of valuable information, including a “formula, pattern, compilation,
program, device, method, technique, or process,” that derives independent economic value from
not being generally known or readily ascertainable and is subject to reasonable efforts by the
owner to maintain its secrecy.3 Examples of trade secrets include blueprints, customer lists,
pricing information, and source code. While protection of patents and copyright is an exclusive
matter of federal law, trade secret protection is found not only in federal law, but also in state law.
Most states have adopted the Uniform Trade Secret Act (UTSA), a model law drafted by the
National Conference of Commissioners on Uniform State Laws.
There are important differences between trade secrets and patents. Individuals do not have to
apply for trade secret protection as they would for patents. Protection of trade secrets originates
immediately with the creation of the trade secret; there is no process for applying for protection or
registering trade secrets. Trade secret protection does not expire unless the trade secret becomes
known. In contrast, patent applicants must disclose information about their innovation to the PTO
in order to acquire a patent. Patents offer right holders stronger protection but for a limited period
of time. While applying for a patent can be a costly and lengthy process, patents are valuable if
the confidentiality of the innovation is fragile or if the area of research is highly competitive.
Copyright
Protection of copyrights in the United States is based on the Copyright Act (17 U.S.C. 101, et
seq.). Copyrights protect original expressions of authorship, fixed in physical and/or digital
2
In some cases, the effective duration of patent protection can be shorter, for example, because of regulatory delays in
the approval of the patent or delays in obtaining marketing approval for the patented invention.
3
Uniform Trade Secret Act, §1(4).
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forms. Such protections include literary or artistic works such as books, music, sound recordings,
movies, paintings, architectural works, and computer software and databases (though not
individual bits of data). Traditionally, copyrights differed from patents in that there was no claim
to industrial applicability or novelty of the idea. The expression of the idea, not the underlying
idea, was being copyrighted. While some of the criteria for copyrights differ from those of
patents, the objective is the same: investments of time, money, and effort to create work of
cultural, social and economic significance should be protected to encourage further creativity.
U.S. law provides copyright protection for life of the author plus 70 years for personal works, or
120 years from creation (or 95 years from publication) for corporate works. Copyrights may be
registered by the U.S. Copyright Office of the Library of Congress, although protection arises
immediately upon fixation in a tangible medium of expression.
Trademarks
Trademark protection in the United States is governed jointly by state and federal law. The main
federal statute is the Lanham Act of 1946 (15 U.S.C. 1051, et seq.). Also known as service marks,
trademarks permit the seller to use a distinctive name, mark, symbol, or sound to identify and
market a product, service, or company. The trademark allows quick identification of the seller’s
product, and for good or ill, can become an indicator of a product’s quality. If for good, the
trademark can be valuable in the introduction of new products by conveying an instant assurance
of quality. The trademark is designed to prevent other companies with similar merchandise from
free-riding on the association of quality with the trademarked item. Thus, a trademarked good
may command a premium in the marketplace because of its reputation. For trademarks,
distinctiveness is at a premium because a trademark must capture the consumer’s imagination to
be effective as generic names of commodities cannot be trademarked. Trademark rights are
acquired through use or through registration with the PTO.
A related concept to trademarks is the geographic indication, which is also protected by the
Lanham Act. The geographic indication acts to protect the quality and reputation of a distinctive
product originating in a certain region; however, the benefit does not accrue to a sole producer,
but rather the producers of a product originating from a particular region. Geographic indications
are generally sought for agricultural products, or wines and spirits. Protection for geographical
indications is acquired in the United States by registration with the PTO, through a process
similar to trademark registration. In general, however, the United States protects geographic
indications through trademark law.
Infringement of IPR
IPR infringement is the misappropriation or violation of the IPR. In the case of patents,
infringement of a patent owner’s exclusive rights (as afforded by patent laws) involves a third
party’s unauthorized use of the patented invention. As relates to international trade, the greatest
challenge to the patent right is infringement in foreign countries, or non-observance by WTO
member states to the minimal standards of the TRIPS Agreement. Copyright infringement occurs
when a third party engages in reproducing, performing, or distributing a copyrighted work
without the consent of the copyright owner. In addition to the term infringement, other terms are
used to describe certain violations of IPR.
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Piracy
The term “piracy” has applications to both copyrights and trademarks. The major challenge
facing copyright protection is piracy, either through physical duplication of the work, illegal
dissemination of copyrighted material (such as computer software, music, or movies) over the
Internet, and/or participation in commercial transactions of copyrighted materials without the
consent of the copyright owner. With respect to trademarks, piracy involves the registration or use
of a famous foreign trademark that is not registered in the country or is invalid because the
trademark has not been used.
Counterfeiting
An imitation of a product is referred to as a “counterfeit” or a “fake.” Counterfeit products are
manufactured, marketed, and distributed with the appearance of being the genuine good and
originating from the genuine manufacturer.4 The purpose of counterfeit goods is to deceive
consumers about their origin and nature. Counterfeiting and copying of original goods are major
challenges for trademarked products. The counterfeited product can be sold for a premium
because of its association with the original item, while reducing the sales of the original items.
Furthermore, consumer experience with a counterfeited good of inferior quality, can damage the
reputation of the trademark product. Popular examples of counterfeit products include fake
fashionwear, such as Louis Vuitton bags or Rolex watches, or fake pharmaceutical products, such
as popular brand-name prescription medicines.
A related issue is the imitation of labels and packaging of trademarked goods. In this situation, the
imitator uses a trademark that is confusingly similar to a well-known trademark in order to
benefit from the reputation of the product with which he is competing.
Innovation Indicators
According to the Organisation for Economic Co-operation and Development (OECD), innovation
is the “implementation of a new or significantly improved product (good or service), or process, a
new marketing method, or a new organizational method.” Innovation is widely considered to be a
key source of economic growth, and IPR to be a major driver of innovation. The measurement of
innovation is an evolving field. Possible elements of innovation indicators include activities
related to the commercialization of inventions and new technologies.5 One such component could
be global trends in patenting.6 Trends in the total number of patent filing applications received
4
Counterfeit goods should be distinguished from generic goods, i.e., in the case of generic forms of pharmaceutical
medicines.
5
National Science Board (NSB), Science and Engineering Indicators 2012, Arlington, VA, 2012, pp. 6-8.
6
The NSB notes the following caveat from W. Cohen, R. Nelson, and J. Walsh, “Protecting Their Intellectual Assets:
Appropriability Conditions and Why U.S. Manufacturing Firms Patent (or Not),” National Bureau of Economic
Research (NBER), Working Paper No. 7552, 2000:
Patenting is an intermediate step toward innovation, and patent data provide indirect and partial indicators of
innovation. Not all inventions are patented, and the propensity to patent differs by industry and technology. Not all
patents are of equal value, and not all foster innovation—patents may be obtained to block rivals, negotiate with
competitors help in infringement lawsuits.
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under the Patent Cooperation Treaty (PCT), an international patent filing system administered by
the World Intellectual Property Organization (WIPO), may be illustrative.
Between 2010 and 2012, the number of patents filed under the PCT grew by nearly 7% (see
Table 1), reflecting economic recovery after the international financial crisis of 2008-2009.7
Intellectual property holdings that are protected by international agreements are highly
concentrated in certain countries. The United States continues to be the source of the world’s
largest number of patent filing applications under the PCT, representing close to one-third of such
filings in 2012. The United States, along with Germany and Japan, accounted for about 60% of all
patent applications filed in 2012 under the PCT. China ranked as the fourth largest source of
international patent filings under the PCT in 2012, representing about 10% of global filings. In
recent years, China has had the highest growth rate in such filings, at about 14% in 2012.
Table 1. Global Intellectual Property Filings Through the PCT, 2010-2012
Country of Origin
2012 Share
(%)
2011-2012
Growth (%)
2010
2011
2012
164,338
182,379
194,400
100.0%
6.6%
United States
45,029
49,060
51,207
26.3%
4.4%
Japan
32,150
38,874
43,660
22.5%
12.3%
Germany
17,568
18,851
18,855
9.7%
0.0%
China
12,296
16,402
18,627
9.6%
13.6%
South Korea
9,669
10,447
11,848
6.1%
13.4%
France
7,246
7,438
7,739
4.0%
4.0%
United Kingdom
4,891
4,848
4,895
2.5%
1.0%
Switzerland
3,728
4,009
4,194
2.2%
4.6%
Netherlands
4,063
3,503
3,992
2.1%
14.0%
Sweden
3,314
3,462
3,585
1.8%
3.6%
Italy
2,658
2,695
2,836
1.5%
5.2%
Canada
2,698
2,945
2,748
1.4%
-6.7%
Finland
2,138
2,079
2,353
1.2%
13.2%
Australia
1,772
1,739
1,708
0.9%
-1.8%
Spain
1,772
1,729
1,687
0.9%
-2.4%
13,346
14,298
14,466
7.4%
1.2%
TOTAL
Others
Source: World Intellectual Property Organization.
7
WIPO, “Strong Growth in Demand for Intellectual Property Rights in 2012,” press release, March 19, 2013,
http://www.wipo.int/pressroom/en/articles/2013/article_0006.html.
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Role of Intellectual Property in U.S. Economy
Intellectual property generally is viewed as a longstanding strategic driver of U.S. productivity,
economic growth, employment, higher wages, and exports. It also is considered a key source of
U.S. comparative advantage, such as in innovation and high-technology products. Nearly every
industry depends on it for its businesses. Among the industries that are dependent on patent
protection are the aerospace, automotive, computer, consumer electronics, pharmaceutical, and
semiconductor industries. Copyright-based industries include the software, data processing,
motion picture, publishing, and recording industries. Other industries that indirectly benefit from
IPR protection include retailers, traders, and transportation businesses, which support the
distribution of goods and services derived from intellectual property.8
IP-intensive industries are considered to play a major role in the U.S. economy and international
trade. What follows are some findings from a study by the U.S. Department of Commerce.9
•
U.S. economic impact. In 2010, a subset of the most intellectual propertyintensive industries directly supported 27.1 million jobs in the United States, or
about 18.8% of total U.S. employment. They also indirectly supported 12.9
million U.S. jobs via the supply chain in other industries. In 2010, the wages of
employees working in IP-intensive industries tended to be about 42% higher on
average than those working in non-IP-intensive industries. These industries
accounted for $5.06 trillion in value added to the U.S. economy, more than onethird of the U.S. gross domestic product (GDP).
•
U.S. trade in goods. In 2010, IP-related merchandise exports amounted to $775
billion (two-thirds of total U.S. merchandise exports), while IP-related
merchandise imports reached $1,336 billion (about 70% of total U.S.
merchandise imports). Key sectors for IP-intensive merchandise trade include
semiconductor and electric parts, basic chemicals, motor vehicles,
pharmaceuticals and medicine, and computer and peripheral equipment.10
•
U.S. trade in services. In 2007, exports of services by IP-intensive industries
totaled about $90 billion (about 19% of total U.S. private services exports). Key
sources of services exports included the software publishing, motion picture and
video, financial services, science R&D, and management and technical
consulting industries. The study does not provide information on imports of
services by IP-intensive industries, though it should be noted that the United
States runs an overall surplus in international trade in services.11
8
Stephen E. Siwek, “Engines of Growth: Economic Contributions of the US Intellectual Property Industries,”
commissioned by NBC Universal, 2005, p. 2.
9
Department of Commerce, Intellectual Property and the U.S. Economy: Industries in Focus, March 2012,
http://www.uspto.gov/news/publications/IP_Report_March_2012.pdf.
10
It is important to note that trade statistics may not capture the full importance of intellectual property (IP)-intensive
products to the U.S. economy, as many IP-intensive products are manufactured abroad as part of the global supply
chain, and the full value added of these products is not accounted for in trade statistics. In addition, services statistics
are limited.
11
CRS Report R43291, U.S. Foreign Trade in Services: Trends and U.S. Policy Challenges, by William H. Cooper.
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The role of IP-intensive industries in U.S. trade in services includes receipts (exports) and
payments (imports) of royalties and licensing fees. Right holders may authorize the use of
technologies, trademarks, and entertainment products that they own to entities in foreign
countries, resulting in revenues through royalties and license fees. In 2012, U.S. receipts from
cross-border trade in royalties and license fees (relating to patent, trademark, copyright, and other
intangible rights) totaled $124.2 billion, up about 3.5% from 2011 receipts of $120.7 billion. At
the same time, U.S. payments of royalties and license fees to foreign countries amounted to $39.9
billion, up about 5% from the 2011 level of $34.8 billion. As with overall U.S. trade in services,
U.S. cross-border trade in royalties and license fees generated a trade surplus—of $84.3 billion in
2012, a small decline from $85.9 billion in 2011. U.S. trade in royalties and licenses accounted
for about 16% of total U.S. trade in private services in 2012.12
Industry-specific figures may further demonstrate the importance of intellectual property to the
U.S. economy. For example:
•
Copyright industries. According to a study commissioned by the International
Intellectual Property Alliance (IIPA), in 2012, industries categorized as part of
the “core” copyright industries (e.g., computer software, videogames, books,
newspapers, periodicals and journals, motion pictures, recorded music, and radio
and television broadcasting) contributed about $1 trillion to the U.S. economy
(“value-added” to current GDP), representing about 6.5% of the U.S. economy.
The study also estimated that the “core” copyright industries employed nearly 5.4
million workers in 2012, representing about 4% of the total U.S. workforce. In
addition, the study estimated that foreign sales of certain U.S. copyright sectors
totaled $142 billion in 2012.13
•
Pharmaceutical industry. In 2012, domestic sales by pharmaceutical companies
that are members of the Pharmaceutical Researchers and Manufacturers of
America (PhRMA) reached an estimated $178 billion, while sales abroad by
PhRMA members totaled about $117 billion.14
Some advocates of civil liberties assert that empirical analysis on the role of IPR in the U.S.
economy may not be fully evaluating the economic and commercial benefits of lawful exceptions
and limitations to exclusive rights. For example, by one estimate, businesses that rely on “fair
use” exceptions to U.S. copyright law contribute $2.2 trillion to the U.S. economy. The “fair use”
doctrine provides limitations and exceptions to the exclusive rights afforded by copyright law. It
permits limited use of copyrighted works without requiring permission from the right holder in
certain cases, examples of which may include news reporting, research, teaching, and library
use.15
12
CRS analysis of data from BEA, U.S. International Services data.
Stephen E. Siwek, Copyright Industries in the U.S. Economy: The 2013 Report, Economists Incorporated, Prepared
for the International Intellectual Property Alliance (IIPA), http://www.iipa.com/pdf/
2013_Copyright_Industries_Full_Report.PDF.
14
PhRMA, 2013 Biopharmaceutical Research Industry Profile, Washington, DC, July 2013, http://www.phrma.org/
sites/default/files/pdf/PhRMA%20Profile%202013.pdf.
15
Thomas Rogers and Andrew Zamosszegi, Fair Use in the U.S. Economy: Economic Contribution of Industries
Relying on Fair Use, Prepared for the Computer & Communications Industry Association (CCIA), 2010. CCIA, “Fair
Use Doctrine Vital for All of Us,” press release, November 18, 2009, http://www.ccianet.org/index.asp?sid=5&artid=
125&evtflg=False. See also CRS Report RL33631, Copyright Licensing in Music Distribution, Reproduction, and
Public Performance, by Brian T. Yeh.
13
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Prevalence and Economic Consequences of
IPR Infringement
Advances in information and technology and declining costs of transportation and
communication, spurred by globalization, have fundamentally changed information and trade
flows. Such changes have created new markets for U.S. exporters, but at the same time, have
been associated with the proliferation of counterfeiting and piracy on a global scale.
Several factors contribute to the growing problem of IPR infringement. While the costs and time
for research and development are high, IPR infringement occurs with relatively low costs and
risks and a high profit margin. According to PhRMA, it takes a pharmaceutical company about 10
to 15 years of R&D to create a new drug, and the average cost to develop a drug in the early
2000s was about $1.2 billion, with costs possibly higher in more recent years. In 2012, PhRMA
member companies collectively spent nearly $49 billion for research and development (domestic
and abroad).16 In contrast, drug counterfeiters can lower production costs by using inexpensive,
and perhaps dangerous or ineffective, ingredient substitutes.
The development of technologies and products that can be easily duplicated, such as recorded or
digital media, also has led to an increase in counterfeiting and piracy. Increasing Internet usage
has contributed to the distribution of counterfeit and pirated products. Additionally, civil and
criminal penalties often are not sufficient deterrents for piracy and counterfeiting. The United
States is especially concerned with foreign IPR infringement of U.S. intellectual property.
Compared to foreign countries, IPR infringements levels in the United States are considered to be
relatively low.17
Limitations on Data Estimating IPR Infringement Costs
Quantification of the economic losses associated with IPR infringement has been a longstanding
focus in the academic, policy, and industry literature. Many experts agree that it is difficult to
quantify the magnitude of IPR theft with any precision. Reasons may include
•
Illicit nature of IPR infringement. Because IPR infringement is illicit and
secretive, tools that are used to measure legitimate business activity cannot
necessarily be used to measure economic losses from IPR infringement. As such,
it may be easier to quantify the positive contribution of copyright industries to
the U.S. economy more precisely than to measure the losses to the U.S. economy
from copyright piracy.
•
Quantifying specific components of economic impact. The economic impact of
IPR infringement depends on a range of factors, including the different types of
infringing goods being sold, the rate at which consumers substitute buying
infringing goods for legitimate goods, and IPR infringement’s deterrence to
16
PhRMA, 2013 Biopharmaceutical Research Industry Profile.
For example, see Global Intellectual Property Center (GIPC), U.S. Chamber of Commerce, Measuring Momentum:
GIPC International IP Index, First Edition, December 2012, http://www.theglobalipcenter.com/measuring-momentumthe-gipc-international-ip-index/.
17
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R&D. It may be difficult to measure precisely these components of the economic
impact of IPR infringement.18
•
Assumptions used to calculate economic impact. Methods for calculating data
on counterfeiting and piracy often involve certain assumptions. Estimates of
losses from IPR infringement can be highly sensitive to how these assumptions
are derived and weighted. The basic economic model employed in some IPR loss
estimates assumes that there is substitutability between pirated and legitimate
goods. For example, under this model, sales of pirated goods may be equated to
revenue losses of legitimate U.S. copyright businesses. Some analysts suggest
that legitimate firms face a competition threat only if the individuals purchasing
IPR-infringing products would be able and willing to purchase the legitimate
product at the price offered when IPR infringement is not present.19 For
consumers in poor developing countries, especially, this assumption may not be
tenable.
•
IPR infringement in the digital environment. While IPR infringement in the
past primarily constituted counterfeiting and piracy of physical goods (such as
optical media and books), in recent years, there has been a growing amount of
piracy taking place through digital mediums (such as illegal downloads of music
and books over the Internet). It may be more complex to measure IPR
infringement that takes place in the digital environment, and in turn, more
difficult to measure the associated economic losses accurately. U.S. trade losses
due to copyright infringement may be higher than reported because estimates
often do not account for all forms of piracy, such as Internet piracy, which is an
increasingly significant contributor to copyright piracy. One study estimates that
nearly 24% of global Internet traffic infringes upon copyright.20
•
Sources of data. Estimates on economic losses from IPR infringement come
from a range of sources, including academic, policy, and industry sources.
According to a U.S. Government Accountability Office (GAO) study, the U.S.
government does not systematically collect data or analyze the impacts of
counterfeiting and piracy on the U.S. economy. In many cases, the federal
government relies on estimates conducted by industry groups. However,
companies may be reluctant to disclose their IPR losses because of possible
reputational and commercial risks, and industry associations may not always
release their proprietary data sources and methods, complicating efforts to verify
such estimates.21
18
National Intellectual Property Rights Coordination Center, Intellectual Property Rights Violations: A Report on
Threats to United States Interests at Home and Abroad, November 2011 (hereinafter, NIPRCC, 2011).
19
Robert G. Picard, “A Note on Economic Losses Due to Theft, Infringement, and Piracy of Protected Works,” Journal
of Media Economics, 17(3), 207-217, 2004.
20
Envisional, Technical Report: An Estimate of Infringing Use of the Internet, January 2011.
21
U.S. Government Accountability Office (GAO), Intellectual Property: Observations on Efforts to Quantify the
Economic Effects of Counterfeit and Pirated Goods, GAO-10-423, April 2010; and Commission on the Theft of
American Intellectual Property, The IP Commission Report.
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International Economic Effects of IPR Infringement
While assessments of the overall global economic costs of IPR infringement are limited, available
evidence indicates that the adverse economic effects of global IPR infringement stand in the
hundreds of billions of dollars, and are increasing.22 Customs data on seizures of counterfeit and
pirated goods may offer some idea of the magnitudes involved in terms of impact on producers
and exporters. A 2007 study by the Organisation for Economic Co-operation and Development
(OECD) indirectly extrapolated available customs data on seizures to conclude that world trade in
counterfeit and pirated goods may have amounted to $200 billion in 2005.23 Updated OECD
estimates suggest that trade in IPR-infringing goods may have totaled up to $250 billion in 2007.
During that same time period, the share of counterfeiting and pirated goods in world trade also is
estimated to have increased—from 1.85% in 2000 to 1.95% in 2007.24
More recently, a study commissioned by the Business Action to Stop Counterfeiting and Piracy
(BASCAP), a business initiative organized by the International Chamber of Commerce, built on
the OECD’s work. According to the BASCAP study, for the G-20 economies, the total value of
counterfeit and pirated products was an estimated $455-$650 billion in 2008, and is projected to
reach $1.22-$1.77 trillion in 2015 (see Table 2).25
In terms of broader economy-wide effects, the BASCAP study estimated that G-20 economies
lost $125 billion every year from counterfeiting and piracy due to additional impacts on trade,
foreign investment, employment, and other factors. In addition, the study estimated that G-20
economies lost about 2.5 million jobs from counterfeiting and piracy; i.e., up to 2.5 million
legitimate jobs could have been created in the absence of counterfeiting and piracy.26
Table 2. Estimated International Economic Losses Due to Counterfeiting and Piracy,
Selected Years
(Billions of U.S. Dollars)
Category
2008
2015
Internationally traded counterfeit and
pirated products
$285-$360
$770-$960
Domestically produced and consumed
counterfeit and pirated products
$140-$215
$370-$570
$30-$75
$80-$240
$455-$650
$1,220-$1,770
Digitally pirated products
Total
Source: Frontier Economics, Estimating the Global Economic and Social Impacts of Counterfeiting and Piracy, A
Report Commissioned by Business Action to Stop Counterfeiting and Piracy (BASCAP), February 2011.
Notes: BASCAP economic loss estimates are restricted to the G-20 economies.
22
NIPRCC, 2011.
OECD, The Economic Impact of Counterfeiting and Piracy, June 2008, http://www.oecd.org/fr/sti/ind/
theeconomicimpactofcounterfeitingandpiracy.htm.
24
OECD, Magnitude of Counterfeiting and Piracy of Tangible Products: An Update, November 2009.
25
Frontier Economics, Estimating the Global Economic and Social Impacts of Counterfeiting and Piracy, A Report
Commissioned by Business Action to Stop Counterfeiting and Piracy (BASCAP), February 2011.
26
Ibid.
23
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U.S. Economic Effects of IPR Infringement
While specific estimates vary, the available data suggest that U.S. economic losses from IPR
infringement could be significant.
Customs Seizure Data
Data on pirated and counterfeit seizures of imports at U.S. borders shed light on the magnitude of
the issue in the U.S. context (see Figure 1). The Department of Homeland Security (DHS) made
22,848 seizures of IPR-infringing goods in FY2012, down from 24,792 seizures in FY2011 but
more than double the FY2005 level of 8,022 seizures. The general trend of the increased number
of seizures over time could reflect a combination of increased DHS enforcement action and
growing levels of counterfeiting and piracy. The total value of DHS seizures, as measured by the
manufacturer’s suggested retail price (MSRP), amounted to $1.26 billion in FY2012, up from
$1.11 billion in FY2011.27 It is worth noting that customs data may be limited in that they do not
reflect digital-based IPR infringement.
Figure 1. Composition of U.S. Border Seizures of Counterfeit and Pirated Goods,
FY2012
Source: Department of Homeland Security (DHS), Intellectual Property Rights: Fiscal Year 2012 Seizure
Statistics.
Of all U.S. trading partners, China continues to account for the majority of counterfeits
intercepted at the U.S. border. In FY2012, seizures of goods originating from China represented
72% of all DHS seizures and $906 million in MSRP value. Other countries that were primary
sources for counterfeit and pirated goods seized included Hong Kong, India, and Singapore.28
27
Department of Homeland Security (DHS), Intellectual Property Rights: Fiscal Year 2012 Seizure Statistics, Prepared
by U.S. Customs and Border Protection (CBP), Office of International Trade, http://www.cbp.gov/linkhandler/cgov/
trade/priority_trade/ipr/ipr_communications/seizure/fy2012_final_stats.ctt/fy2012_final_stats.pdf.
28
Ibid.http://www.cbp.gov/linkhandler/cgov/trade/priority_trade/ipr/ipr_communications/seizure/
fy2012_final_stats.ctt/fy2012_final_stats.pdf
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A top priority for the CBP is seizing counterfeit imports that endanger the health and safety of
consumers, such as counterfeit healthcare products, pharmaceutical products, and consumer
electronics. The total MSRP value of IPR-related seizures of commodities that represent a
potential safety and security risks was about $146 million (3,402 seizures) in FY2012, down from
$196 million (4,369 seizures) in FY2011. Pharmaceutical goods were the top commodity
category posing safety and security risks, accounting for more than half of such seizures by both
MSRP value ($83 million) and number of seizures (2,343).29
Economic Loss Estimates
U.S. industries that rely on IPR protection claim to lose billions of dollars in revenue annually
due to piracy and counterfeiting. Beyond these direct losses, the United States may face
additional “downstream” losses from counterfeiting and piracy. IPR infringement could result in
the loss of jobs that would have been created if the infringement did not occur, which could
translate into lost earnings by U.S. workers and, in turn, lost tax revenues for federal, state, and
local governments.30 Attempts have been made in specific economic sectors to quantify the IPR
infringement levels and related losses to legitimate U.S. businesses.
Overall U.S. Estimates
The BASCAP study (discussed in the international section) used its global findings to determine
the impact of global counterfeiting and piracy on the United States (see Table 3). BASCAP
estimated that the United States consumes $66-$100 billion in domestically produced counterfeit
and pirated goods annually (based on 2008 data). In terms of specific industries, BASCAP
estimated that the United States consumes $7-$20 billion worth of digitally pirated recorded
music and $1.4-$2 billion in digitally pirated movies in 2005.
Table 3. Estimated U.S. Economic Losses Due to Counterfeiting and Piracy
(Billions of U.S. Dollars)
Category
Loss Estimate (based on 2008 data)
Internationally traded counterfeit and pirated products
$45-$60
Domestically produced and consumed counterfeit and pirated products
$12-$14
Digitally pirated products
$9-$25
Total
$66-$100
Source: Frontier Economics, Estimating the Global Economic and Social Impacts of Counterfeiting and Piracy, A
Report Commissioned by Business Action to Stop Counterfeiting and Piracy (BASCAP), February 2011.
A private Commission on the Theft of American Intellectual Property estimates the total level of
U.S. economic losses to international theft of U.S. intellectual property to be even higher, at
29
Ibid.
There may be limitations on data estimating the impact of counterfeiting and piracy on the U.S. economy. Some
critics point out that many of the estimates for losses associated with IPR infringement are generated by industry
groups that may have self-interested motivations.
30
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hundreds of billions dollars per year. The Commission says the level of losses is comparable to
the size of U.S. exports to Asia in 2012, valued at $320 billion.31
Sectoral Estimates
Attempts also have been made in some intellectual property-based industries to quantify the IPR
infringement levels and related losses to legitimate U.S. businesses. For example, in prior years,
IIPA, a U.S. copyright industry association, and PhRMA, a U.S. pharmaceutical industry
association, have calculated estimates of losses to their member companies from IPR
infringement. However, in recent years, neither of these industry groups has provided estimates.
This may be, in part, because of the growing complexities in calculating the impact of such losses
because of trends such as increased piracy taking place through the Internet.
The Organizational Structure of IPR Protection
Given the importance of intellectual property to the U.S. economy and the economic losses
associated with counterfeiting and piracy, the United States is a leading advocate of strong global
IPR rules. Since the mid-1980s, the United States has integrated IPR policy in its international
trade policy activities, pursuing enhanced IPR laws and enforcement through multilateral,
regional and bilateral trade agreements, and national trade laws.
Multilateral IPR System
World Trade Organization (WTO)
At the center of the present multilateral trading system is the World Trade Organization (WTO),
an international organization established in 1995 as the successor to the General Agreements on
Tariffs and Trade (GATT).32 The WTO was established as the result of the Uruguay Round of
trade negotiations (1986-1994), which led to agreements to liberalize and establish or enhance
rules on trade in goods, services, agriculture, and other non-tariff barriers to trade. One of the
Uruguay Round agreements was the Agreement on Trade-Related Aspects of Intellectual Property
Rights (TRIPS Agreement), which sets minimum standards on intellectual property rights
protection and enforcement with which all WTO member states must comply. The United States,
the European countries, and the IPR business community were instrumental in including IPR on
the Uruguay Round agenda. Many developing countries were wary of including IPR in trade
negotiations, preferring to discuss them under the World Intellectual Property Organization
(WIPO) (see below) instead. However, developing countries agreed, after being granted delayed
compliance periods, and after achieving negotiating goals on other issues such as the end of
quotas on textiles and clothing.
While previous international treaties on IPR continue to exist, the TRIPS Agreement was the first
time that intellectual property rules were incorporated into the multilateral trading system. Two
basic tenets of the TRIPS Agreement are national treatment (signatories must treat parties of other
31
32
Commission on the Theft of American Intellectual Property, The IP Commission Report.
The GATT was originally established in 1947.
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WTO members no less favorably in terms of IPR protection than the party’s own nationals) and
most-favored-nation treatment (any advantage in IPR protection granted to the party of another
WTO member shall be granted to nationals of all other WTO member states).
Much of the TRIPS Agreement sets out the extent of the agreement’s coverage of the various
types of intellectual property: patents, copyrights, trademarks, trade secrets, geographical
indications, industrial designs, layout of circuitry design, and test data. The TRIPS Agreement
provisions build on several existing IPR treaties administered by the WIPO (discussed below).
Another part provides standards of enforcement for IPR covered by the agreement. It enumerates
standards for civil and administrative procedures and remedies, the application of border
measures, and criminal procedures. A Council for the TRIPS Agreement was established to
monitor the implementation of the agreement and transition arrangements were devised for
developing countries. Finally, the agreement provides for the resolution of disputes under the
Uruguay Round Agreement’s Dispute Settlement Understanding (see text box). The binding
nature of the WTO dispute settlement mechanism, with the possibility of the withdrawal of trade
concessions (usually the reimposition of tariffs) for non-compliance, sets this agreement apart
from previous IPR treaties that did not have effective dispute settlement mechanisms.
U.S. WTO Cases Against China on IPR
In April 2007, the United States filed two WTO dispute settlement cases against China, alleging inadequacies in
China’s enforcement of IPR laws and its barriers to market access for U.S. copyright businesses.33
In January 2009, the WTO issued its final ruling on the case centering on IPR enforcement issues. The WTO panel
ruled in the United States’ favor that China’s denial of copyright protection to works without censorship approval is
inconsistent with the TRIPS Agreement. The panel also agreed with the United States that it is impermissible for
China to publicly auction IPR-infringing goods seized at the border, with the only requirement being that fake brands
and trademarks be removed from the goods. The WTO panel ruled that more evidence was needed before deciding
whether the thresholds for prosecution of counterfeiting and piracy in China’s criminal law permit commercial scale
IPR infringement. China agreed to implement the WTO ruling.34
In August 2009, a WTO panel ruled that a number of China’s restrictions on trading rights and distribution of IPRrelated products were inconsistent with WTO rules. However, the WTO panel did not address whether China’s
censorship policies or import limitations on foreign films violate WTO rules. China agreed to implement the WTO
ruling.35
The TRIPS Agreement also seeks a balance of rights and obligations between protecting private
right holders and the obligation “to secure social and cultural development that benefits all.”36
Article 7 declares that
... the protection and enforcement of IPR should contribute to the promotion of technological
innovation and to the transfer and dissemination of technology, to the mutual advantage of
33
USTR, “United States Files WTO Cases Against China Over Deficiencies in China’s Intellectual Property Rights
Laws and Market Access Barriers to Copyright-Based Industries,” press release, April 9, 2007, http://www.ustr.gov.
See also CRS Report RL33536, China-U.S. Trade Issues, by Wayne M. Morrison.
34
WTO, “WTO issues panel report on U.S.-China dispute over intellectual property rights,” press release, January 26,
2009. USTR, “United States Wins WTO Dispute Over Deficiencies in China’s Intellectual Property Rights Law,” press
release, January 26, 2009. Daniel Pruzin, “WTO Publishes Final Ruling in U.S. Complaint Against Chinese IPR
Enforcement Measures,” International Trade Daily, January 27, 2009.
35
See CRS Report RL33536, China-U.S. Trade Issues, by Wayne M. Morrison.
36
Pascal Lamy, “Trade-Related Aspects of Intellectual Property Rights - Ten Years Later,” Journal of World Trade,
October 2004, p. 925.
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producers and users of technological knowledge and in a manner conducive to social and
economic welfare and to a balance of rights and obligations.
This paragraph attempts to link the protection of IPR with greater technology transfer, including
technology covered by IPR protection, to the developing world. The language itself has been
interpreted in various ways. Developed countries have tended to consider this language
exhortatory, but developing countries have tried, without much success, to make technology
transfer a meaningful obligation within the TRIPS Agreement system. Article 66.2 of the
agreement requires developed country members to provide incentives to their enterprises and
institutions to promote technology transfer to least-developed countries to assist them in
establishing a viable technology base. Developed countries report annually on their efforts to
encourage technology transfer.
Complying with international IPR standards may impose greater burdens on developing countries
than developed countries. Developing countries generally have to engage in greater efforts to
bring their laws, judicial processes, and enforcement mechanisms into compliance with the
TRIPS Agreement. Consequently, developing countries were given an extended period of time in
which to bring their laws and enforcement mechanisms into compliance with the TRIPS
Agreement. Developing countries and post-Soviet states were given an additional four years from
the entry into force of the agreement (January 1, 1995). For products that were not covered by a
country’s patent system (such as pharmaceuticals in many cases), an additional five years was
granted to bring such products under coverage. For developing countries, all provisions of the
TRIPS agreement should now be in force. For the least developed countries, the phase-in period
for IPR commitments was originally extended 10 years to January 1, 2006 (Article 66.1). In 2002,
the WTO extended IPR obligations for least developed countries with respect to pharmaceuticals
to January 1, 2016.37 In addition, the WTO has extended the overall transitional period twice—in
2005, an extension to July 1, 2013, and then in 2013, a further extension to July 1, 2021.38 Article
66.1 acknowledges the:
special needs and requirements of least-developed country Members, their economic,
financial and administrative constraints, and their need for flexibility to create a viable
technological base.
Declaration on TRIPS Agreement and Public Health
In agreeing to launch the Doha Round of WTO trade negotiations, trade ministers adopted a
“Declaration on the TRIPS Agreement and Public Health” on November 14, 2001.39 The
Declaration sought to alleviate developing country dissatisfaction with aspects of the TRIPS
regime (see text box). It delayed the implementation of patent system provisions for
pharmaceutical products for least developed countries until 2016. The declaration committed
member states to interpret and implement the agreement to support public health and to promote
access to medicines for all. The Declaration recognized certain “flexibilities” in the TRIPS
37
“Extension of the Transition Period under Article 66.1 of the TRIPS Agreement for Least-Developed Country
Members for Certain Obligations with Respect to Pharmaceutical Products,” WTO Document IP/C/25, July 1, 2002.
38
WTO TRIPS Council, “Extension of the Transition Period Under Article 66.1 for Least Developed Country
Members,” June 12, 2013.
39
Declaration on the TRIPS Agreement and Public Health, (WT/MIN(01)/DEC/2), November 14, 2001, available at
http://www.wto.org/english/thewto_e/minist_e/min01_e/mindecl_trips_e.htm.
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agreement to allow each member to grant compulsory licenses40 for pharmaceuticals and to
determine what constitutes a national emergency, expressly including public health
emergencies such as HIV/AIDS, malaria, and tuberculosis or other epidemics.
Intellectual Property Protection and Development
The controversy over the relationship between IPR and development was engaged by the advent of the TRIPS
Agreement, which for the first time placed IPR obligations on developing countries. Some hold that expansion of IPR
is an obstacle to growth and development in less advanced countries, while others maintain that IPR are beneficial to
both developed and developing countries.
Some IPR critics believe that a strong IPR regime may reduce developing countries’ access to technology from
advanced countries by imposing relatively higher fees for technology licenses and production rights than would occur
in the absence of IPR, limiting their innovation and economic growth and development. For instance, Japan, Singapore,
Taiwan, and South Korea enhanced their technological abilities and developed their economies through “reverse
engineering” of foreign technologies.
Others claim that IPR promote technology transfer through increased trade, foreign investment, and licensing in the
long-run by making a country more attractive to foreign partners. A 2002 OECD study concluded that stronger IPR
laws, particularly enhanced patent standards, may be associated with increased foreign direct investment (FDI) and
trade for developing countries over time, with variation by industries and level of development.41 For instance, India
experienced an increase in foreign investment and technology transfer once it expanded its patent protection.
However, in recent years, India has taken measures considered by the U.S. government and business leaders to be a
“backsliding” on IPR commitments, raising concerns about the country’s IPR and innovation environment. China offers
a counterexample of a country that, despite some improvements, continues to have a weak IPR regime but high FDI
and trade levels.
There is also evidence that IPR’s impact on developing countries may vary by the level of development. One study
suggests that IPR protection may offer more benefits for the more industrialized developing countries, such as Brazil
and India, compared to other developing countries. Such industrializing economies could experience economic
growth of as much as 0.5% annually through increased trade, FDI, and licensing.42 Another study finds that rapid
economic growth is associated with weak intellectual property regimes, but that developing countries with higher
levels of per capita income may benefit economically from stronger IPR regimes.43
There is also concern that strengthened patent protection may drive up prices for medicines or delay the entry of
generic drugs into the market, reducing access to HIV/AIDS treatments and other drugs. IPR supporters argue that
strong IPR is critical to creating incentives for pharmaceutical innovations and suggest that reduced prices are no
guarantee that needed goods will make it into the hands of individuals in developing countries due to political
corruption, poverty, lack of health care, and poor social infrastructure.
Paragraph 6 of the Doha Declaration directed the WTO members to formulate a solution to a
corollary concern, the use of compulsory licensing by countries with insufficient or inadequate
manufacturing capability. Compulsory licenses are issued by governments to authorize the use or
production of a patented item by a domestic party other than a patent holder. They are authorized
by Article 31 of TRIPS, which places certain limitations on their use, scope, and duration. A
provision that predominantly restricted production authorized by compulsory license to the
40
Compulsory licenses are issued by governments to authorize the use of or production of a patented item by a
domestic party other than a patent holder.
41
OECD, The Impact of Trade-Related Intellectual Property Rights on Trade and Foreign Direct Investment in
Developing Countries, May 28, 2003, p. 21, http://www.oecd.org.
42
Keith E. Maskus, Intellectual Property Rights in the Global Economy, Institute for International Economics (IIE),
Washington, D.C., August 2000.
43
Commission on Intellectual Property Rights (CIPR), Integrating Intellectual Property Rights and Development
Policy, September 2002.
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domestic market became the focal point of the negotiations because it, in effect, conveys the right
of compulsory licensing only to countries with the capability to manufacture a given product.
Countries without a domestic manufacturing capability were essentially precluded from using this
flexibility of the TRIPS agreement.
On the eve of the Cancun Ministerial in August 2003, WTO members agreed on a Decision44 to
waive the domestic market provision of the TRIPS article on compulsory licensing (Article 31(f))
for exports of pharmaceutical products for “HIV/AIDS, malaria, tuberculosis and other
epidemics” to least developed countries and countries with insufficient manufacturing capacity.
This Decision was incorporated as an amendment to the TRIPS agreement at the Hong Kong
Ministerial in December 2005.
The amendment must be ratified by two-thirds of the 153 WTO member states. The deadline for
ratification has been extended a number of times, most recently, until December 31, 2015.45 Until
then, the 2003 waiver continues in force. To date, the United States and 76 other WTO members
have ratified the amendment.46 This means another 25 countries must ratify the amendment to
reach the two-thirds threshold.
The system established by the WTO allows least developed countries and countries without
sufficient manufacturing capacity to issue a compulsory license to a company in a country that
can produce such a product. After a matching compulsory license is issued by the producer
country, the drug can be manufactured and exported subject to various notification requirements,
as well as quantity and safeguard restrictions. While several exporting countries have established
laws and procedures for implementing this system, only Rwanda has availed itself of the system
to import HIV/AIDS medicines from a generic manufacturer in Canada.47
World Intellectual Property Organization (WIPO)
In addition to the WTO, the other main multilateral venue for addressing IPR issues is the World
Intellectual Property Organization (WIPO), a specialized agency affiliated with the United
Nations with its own executive, legislative, and budgetary powers. Established in 1970, following
the entry into force of the 1967 WIPO Convention, WIPO is charged with fostering the effective
use and protection of intellectual property globally. WIPO’s mandate focuses exclusively on
intellectual property, in contrast to the WTO’s broader international trade mandate. WIPO’s
antecedents are the 1883 Paris Convention for the Protection of Industry Property and the 1886
Berne Convention for the Protection of Literary and Artistic Work. Most of the substantive
provisions of these two treaties are incorporated in the WTO’s TRIPS Agreement. WIPO’s
primary function is to administer a group of IPR treaties which put forth minimum standards for
44
“Implementation of Paragraph 6 of the Doha Declaration on the TRIPS Agreement and Public Health,” IP/C/W/405,
August 30, 2003, and accompanying Chairman’s statement, available at http://www.wto.org/english/news_e/pres03_e/
pr350_e.htm.
45
WTO, “Intellectual property meeting mulls Irish tobacco plan, drug tariffs, sport, non-violation, press release,
October 10 and 11, 2013.
46
“Members accepting amendment of the TRIPS Agreement,” http://www.wto.org/english/tratop_e/trips_e/
amendment_e.htm.
47
“Canada Issues Compulsory License For HIV/AIDS Drug Export To Rwanda, In First Test Of WTO Procedure,”
Bridges Weekly Trade News Digest, September 26, 2007, http://www.ictsd.org/weekly/07-09-26/story2.htm.
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member states (see Appendix A). All international IPR treaties, save TRIPS, are administered by
WIPO.
In order to address digital technology issues not dealt with in the TRIPS Agreement, WIPO
established the WIPO Copyright Treaty (WCT) and WIPO Performance and Phonograms Treaty
(WPPT) in 1996, oftentimes collectively referred to as the “WIPO Internet Treaties.”48 Recent
WIPO efforts have focused on patent law. In June 2000, WIPO signatories adopted the Patent
Law Treaty (PLT), which called for harmonization of patent procedures. This agreement went
into force on April 28, 2005. Discussions began in May 2001 for the Substantive Patent Law
Treaty (SPLT), which targets issues specifically related to patent grants, but were put on hold in
2006. Government leaders participating in the Group of 8 (G-8) meeting in July 2008 called for
“accelerated discussions” of the SPLT.49 While discussions remain stalled, the main focus of the
WIPO’s work in this area has been on “building a technical and legal resource base from which to
hold informed discussions in order to develop a work program” on various patent issues.50
WIPO’s other functions include assisting member states through training programs, legislative
information, intellectual property institutional development, automation and office modernization
efforts, and public awareness activities. WIPO’s enforcement activities are more limited than
those of the WTO. Through its Advisory Committee on Enforcement (ACE), WIPO cooperates
with member states to promote international coordination on enforcement activities.
Free Trade Agreements
In recent years, the United States increasingly has focused on free trade agreements (FTAs) as an
instrument to promote stronger IPR regimes by foreign trading partners. In general, the United
States has viewed the TRIPS Agreement and WIPO-administered treaties as a minimum standard
and has pursued higher IPR protection and enforcement levels through regional and bilateral
FTAs. To date, the United States has entered into 14 FTAs with 20 countries.
Trade Promotion Authority and Negotiating Objectives
Under Trade Promotion Authority (TPA), Congress delegates its constitutional authority to
regulate foreign commerce to the President to negotiate and enter into certain free trade
agreements (FTAs). TPA also includes provisions allowing implementing bills for trade
agreements to be considered under expedited legislative procedures (no amendment, up-or-down
vote), provided the President follows the guidelines, negotiating objectives, reporting, and
consultation requirements mandated by Congress.51 IPR issues have become important
negotiating objectives in grants of TPA; the most recent extension of that authority expired on
July 1, 2007.
48
These WCT and WPPT frequently are referred to as the WIPO Internet Treaties.
Monika Ermert, “G8 Governments Want ACTA Finalised This Year, SPLT Talks Accelerated,” Intellectual
Property Watch, July 9, 2008.
50
WIPO, “Standing Committee on the Law of Patents (SCP),” http://www.wipo.int/policy/en/scp/.
51
See CRS Report RL33743, Trade Promotion Authority (TPA) and the Role of Congress in Trade Policy, by William
H. Cooper.
49
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IPR negotiating objectives for FTAs were first enacted in trade promotion authority (then known
as fast-track authority) by the Omnibus Trade and Competitiveness Act of 1988 (P.L. 100-418).
The act sought enactment and enforcement of adequate IPR protection from negotiating partners.
It also sought to strengthen international rules, dispute settlement, and enforcement procedures
through the GATT and other existing intellectual property conventions. This negotiating mandate
led to the establishment of the TRIPS Agreement during the Uruguay Round and the IPR
provisions in the North American Free Trade Agreement (NAFTA). In the period since the 1988
Act, the IPR provisions of NAFTA and the TRIPS agreement became the template for other
bilateral or regional FTAs. Thus, the focus of IPR negotiating objectives shifted from creating to
strengthening the IPR trade regime.
2002 Trade Promotion Authority
FTA negotiations concluded under the George W. Bush Administration were conducted under the
Trade Promotion Authority Act of 2002 (P.L. 107-210). The principal negotiating objectives with
regards to IPR included
•
Furthering adequate and effective protection of IPA through accelerated and full
implementation of the TRIPS agreement and by ensuring FTAs negotiated by the
United States “reflect a standard of protection similar to that found in U.S.
law”52;
•
Protecting IPR related to new technologies and distribution methods, and
facilitating legitimate digital trade;
•
Eliminating discriminatory treatment in the use and enforcement of IPR;
•
Ensuring adequate rights holder protection through digital rights management
practices; and
•
Providing strong enforcement of IPR.
These IPR negotiating objectives were highly significant to the future contours of U.S. FTA
negotiations. The objective to negotiate trade agreements in terms of IPR that “reflect a standard
of protection similar to that found in U.S. law” led to the negotiation of provisions that go beyond
the level of protection provided in the TRIPS agreement. Often referred to as “TRIPS-plus”
provisions, these obligations include expanding coverage to new sectors; establishing more
extensive standards of protection; and reducing the flexibility options available in TRIPS, such as
with respect to compulsory licensing. Some of the new measures also address technological
innovations that have come about since the TRIPS Agreement.
The objective to apply existing IPR protections to digital media reflected the changing nature of
global commerce. The language sought to extend provisions for IPR protection to new and
emerging technologies and methods of transmission and dissemination. The language also called
for standards of enforcement to keep pace with technological change and allow right holders legal
and technological protections for their works over the Internet and other new media.
52
P.L. 107-210, Sec. 2102(b)(4).
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May 10, 2007, Bipartisan Trade Agreement
On May 10, 2007, the Bush Administration and Congress concluded a bipartisan agreement on
trade policy that addressed some Members’ concerns about the implications of enhanced IPR on
developing countries’ ability to meet public health needs (commonly referred to as the “May 10th
Agreement”).53 In particular, congressional leadership sought to ensure that pending FTAs
allowed trading partners enough flexibility to meet their IPR obligations and to be able to
promote access to life-saving medicines, while otherwise meeting their international IPR
protection and enforcement obligations. IPR language previously negotiated in the FTAs with the
developing countries of Peru, Panama, and Colombia subsequently was modified to reflect the
agreement. Because South Korea is an industrialized country, the United States did not
significantly scale-down the patent protection obligations in the U.S.-Korea FTA.
Possible TPA Renewal
TPA in the form of the Bipartisan Congressional Trade Priorities Act of 2014 (BCTPA) (H.R.
3830/S. 1900) was introduced on January 9, 2014. The principal negotiating objectives in BCTPA
with regards to intellectual property rights are similar to those of the TPA in 2002 (see above).
In addition, a new objective in the proposed BCTPA seeks to negotiate the prevention and
elimination of government involvement in violations of IPR such as cybertheft or piracy. A
related protection of trade secrets and proprietary information collected by governments in the
furtherance of regulations are contained in the negotiating objective on regulatory coherence.
Finally, the proposed legislation reaffirms the Declaration on the TRIPS Agreement and Public
Health and adds language to “foster innovation and access to medicine.” It does not specifically
refer to the patent protection provisions found in the May 10, 2007, Bipartisan Trade Agreement
(discussed above) and the added language seemingly could be used to justify including or
excluding those provisions in future FTAs.
IPR in Current Trade Negotiations
Trans-Pacific Partnership FTA
The Obama Administration is conducting negotiations with participants in the Trans-Pacific
Partnership (TPP) Agreement—Australia, Brunei, Canada, Chile, Japan, Malaysia, Mexico, New
Zealand, Peru, Singapore and Vietnam.54 The objective is to build a comprehensive, high-standard
reciprocal agreement to reduce and eliminate trade barriers and establish rules and disciplines to
govern trade and investment in the region, and to expand and strengthen U.S. economic ties with
other participating countries in the region. Through the TPP, the United Seeks to build on already
established FTAs with Australia, Canada, Chile, Mexico, Peru, and Singapore.20
53
The May 10, 2007, bipartisan trade agreement is available online at http://www.ustr.gov/assets/Document_Library/
Fact_Sheets/2007/asset_upload_file127_11319.pdf.
54
See CRS Report R42694, The Trans-Pacific Partnership (TPP) Negotiations and Issues for Congress, coordinated
by Ian F. Fergusson.
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The United States is negotiating strong IPR provisions in the TPP consistent with the TPA
mandate to “reflect a standard of protection similar to that found in U.S. law.” On the
controversial issue of additional patent protection for pharmaceuticals (e.g., patent term
extension, patent linkage, data protection), the United States reportedly has offered a plan similar
to the May 10th provision: to allow for optional implementation for developing countries in the
TPP and mandatory provisions for developed ones, although certain details have yet to be worked
out.55
IPR reportedly has been one of the more controversial chapters in the TPP negotiating text.
Significant disagreement reportedly continues to exist between and among the parties negotiating
the TPP such as in the areas of:
•
Copyrights: Debate over the extension of copyright term lengths, protection of
temporary copies, fair use provisions, Internet services provider liability, and
anti-circumvention protection;
•
Patents: Debate over the ability to patent plants and animal life, the ability to
patent new uses for an existing product (e.g, “evergreen” patents), and data
exclusivity for biologics, among other issues; and
•
Enforcement: Debate over criminal penalties for trademark counterfeit and
copyright piracy, as well as ex officio powers to seize suspected counterfeit goods
in transit.56
Transatlantic Trade and Investment Partnership FTA
The Obama Administration also is conducting negotiations with the European Union (EU) on a
comprehensive and high-standard free trade agreement, referred to as the proposed Transatlantic
Trade and Investment Partnership (TTIP).57 The United States and EU both maintain strong IPR
standards and generally prioritize IPR protection and enforcement as a key trade negotiating
objective. However, a final report by the U.S.-EU High Level Working Group on Jobs and
Growth, which recommended the launch of the transatlantic FTA negotiations, suggested that it
may be difficult to reconcile differences on the IPR obligations that each side typically includes in
its FTAs.58 For example, protection and enforcement of geographical indications could be
controversial in the negotiations. The EU seeks strong GI protection because of their commercial
value to EU producers (e.g., Parmesan cheese, Parma ham, Feta cheese, and Champagne). The
United States tends to protect GIs through trademark law, and expresses concern that the EU
55
USTR Blog Post, November 29, 2013, http://www.ustr.gov/about-us/press-office/blog/2013/November/stakeholderinput-sharpens-focuses-us-work-on-pharmaceutical-IP-in-TPP
56
Henry Farrell, “Five Key Questions – and Answers- About the Leaked TPP Text,” Washington Post Blog, November
15, 2013 http://www.washingtonpost.com/blogs/monkey-cage/wp/2013/11/15/five-key-questions-and-answers-aboutthe-leaked-tpp-text/; and Electronic Frontier Foundation, “TPP Leak Confirms the Worst: U.S. Negotiators Still Trying
to Trade Away Internet Freedoms,” https://www.eff.org/deeplinks/2013/11/tpp-leak-confirms-worst-us-negotiatorsstill-trying-trade-away-internet-freedoms.
57
See CRS Report R43158, Proposed Transatlantic Trade and Investment Partnership (TTIP): In Brief, by Shayerah
Ilias Akhtar and Vivian C. Jones.
58
U.S.-EU High Level Working Group on Jobs and Growth, Final Report of the U.S.-EU High Level Working Group
on Jobs and Growth, February 11, 2013, http://www.ustr.gov/about-us/press-office/reports-and-publications/2013/
final-report-us-eu-hlwg.
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approach to GIs raises national treatment issues and adversely affects trademarks and widely
accepted generic products.59
Stakeholders on both sides could raise issues about how to balance IPR protection and
enforcement with other public policy goals, such as access to medicines in poor or developing
countries and the free flow of information. At the same time, the TTIP could lead to rules on trade
secrets, an area of U.S. and EU concern in light of increased instances of trade secret theft
internationally, including through cybercrime.60
Anti-Counterfeiting Trade Agreement
The Anti-Counterfeiting Trade Agreement (ACTA), which was negotiated outside of the WTO by
the United States and nearly 40 other primarily developed countries, is intended to build on the
TRIPS Agreement, such as by addressing new IPR issues in the digital environment. Concluded
in 2010, the ACTA has not entered into force. The agreement’s prospects are in question,
following the European Parliament’s rejection of it in 2012, amid widespread protests by
advocates of Internet free speech. The ACTA needs instruments of ratification, acceptance, or
approval from six signatories in order to enter into force. To date, Japan is the only party that has
submitted a formal instrument of approval. IPR issues considered in the ACTA negotiations have
reemerged in in the TPP and TTIP negotiations, making the ACTA of continued congressional
interest.
Central IPR Standards in U.S. FTAs
What follows is a discussion of some of the central patent and copyright standards sought in
FTAs that are currently in force or have been signed by the United States (see Appendix B).61
Patents
Patent protection is arguably one of the most contentious areas of U.S. FTA negotiations on IPR
issues. While the United States and other developed countries advocate for strong patent
protections in order to promote innovation, there is concern that such stringent protections may
delay developing countries’ access to, and increase prices of, generic drugs. Other issues also
have emerged in patent debates, such as with respect to the patentability of innovations related to
plants and animals (see text box). Many of the FTAs in force include TRIPS-plus patent
provisions, the most prominent of which are patent term length extensions, linkages between
regulatory authority and patent status, data protection, compulsory licensing and parallel
importation. The FTAs with Peru, Panama, and Colombia respond to the concerns of some
Members of Congress over provisions that could restrict access to medicines in these countries
59
USTR, 2012 National Trade Estimate Report on Foreign Trade Barriers, p. 148, http://www.ustr.gov/about-us/
press-office/reports-and-publications/2012-1.
60
Executive Office of the President, Administration’s Strategy on Mitigating the Theft of U.S. Trade Secrets, February
2013, http://www.whitehouse.gov//sites/default/files/omb/IPEC/
admin_strategy_on_mitigating_the_theft_of_u.s._trade_secrets.pdf.
61
For a more detailed discussion of the differences between the TRIPS Agreement and regional FTAs that are in force,
see CRS Report RL33205, Intellectual Property and the Free Trade Agreements: Innovation Policy Issues, by John R.
Thomas.
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and contain less ambitious standards for pharmaceutical patents, compared to previously
negotiated FTAs. Pharmaceutical industry advocates express concern that this modification in
patent protection in these FTAs may set a precedent for future FTA negotiations.62 How these
issues will be addressed in the proposed TPP and TTIP continue to evolve. Some key patent
issues are discussed below.
Patent Term Extensions. Many FTAs include provisions for mandatory patent term length
extensions beyond the TRIPS Agreement obligation of patent protection terms of twenty years
from the filing date. These FTAs allow for extensions in cases of “unreasonable” delays in the
issuance of patents due to regulatory review or administrative process, which lessen the effective
20-year term of patent protection. Patent holders contend that such measures enhance the ability
of rights-holders to recoup the costs of research and development of new products. However,
there is concern that patent term extensions may delay the entry of generic drugs into a market. In
a modification of TRIPS-plus obligations, FTAs with Peru, Colombia, and Panama state that
patent term restorations for pharmaceutical products are optional.
Patent Linkages. Patent linkage is a common provision in the trade agreements obtained by the
United States. In general, the term “patent linkage” refers to the attachment of regulatory
approval for the marketing of a drug with the status of a patent. If a patent exists, the Food and
Drug Administration and its counterparts in other countries may not grant marketing approval for
a generic version of a drug that is patented in the country without the permission of the patent
holder. The notion of patent linkage presents a departure from the minimum standards under
TRIPS, under which generic drug manufacturers are able to apply for marketing approval without
the patent owner’s permission and prior to the expiration of the patent; this may reduce the time it
takes for generic drugs to enter a market once the patent expires.63 In light of developing country
concerns about delays in access to generic versions of drugs, FTAs signed with Peru, Panama,
and Colombia do not tie marketing approval for a generic drug with the patent status of its brand
name drug.
Data Protection. In cases in which the patent holders must submit undisclosed data regarding the
safety or efficacy of new pharmaceutical or agricultural products (such as data from clinical
trials) in order to market them, the TRIPS Agreement requires members to take measures to
protect such data from disclosure and unfair commercial use. The TRIPS Agreement does not
prescribe any time period for this protection. Recent U.S. FTAs generally require a five-year
period of marketing exclusivity for the patent holder, which typically begins from the date the
product is approved in the country. Under this TRIPS-plus provision, generic drug manufacturers
who want to market and distribute a generic version of a drug while the data exclusivity period is
in effect must conduct their own clinical trials and submit their own findings to the national drug
regulatory authority; they cannot rely on the findings submitted by the patent holder. On one
hand, clinical trials and other testing used to develop the data submitted for marketing approval
can be costly and take years to develop, and thus, adequate protection of test data is important as
an incentive for future investments in such R&D. On the other hand, such provisions may raise
the cost of manufacturing generic versions of patented drugs, as well as delay access to generic
62
“Brand-Name Industry Alarmed at IPR Precedent of FTA Template,” Inside US Trade, May 18, 2007.
While TRIPS does not directly speak to the rights of generic drug manufacturers in obtaining marketing approval for
a generic drug before the expiration of the patented drug, Article 30 of TRIPS permits exceptions of patent rights for
activities such as “research, prior user rights, and pre-expiration testing.”
63
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forms of drugs. The FTAs with Peru, Panama, and Colombia include provisions that may reduce
data exclusivity terms of five years by a minimum of six months in practice.64
Compulsory Licensing. A compulsory license is an authorization by a government for third
parties (such as a company or the government itself) for the manufacture or use of a product
under patent without the permission of the rights- holder. The TRIPS Agreement permits
signatories to issue compulsory licenses for patented devices and provide compensation to the
owner of the patent and does not limit the situations in which such licenses may be issued. The
third party must have attempted to obtain permission from the patent holder, although this
requirement is waived in times of national emergency or other extenuating circumstances. U.S.
FTAs with Australia and Singapore limit attaining compulsory licenses only for domestic use and
to situations of remedying antitrust violations or in situations of public non-commercial use,
national emergency, or other cases of extreme need. Also under these FTAs, the patent holder is
under no obligation to provide test data, technical know-how or other undisclosed information for
the patent subject to compulsory license. The compulsory license provisions have not been
included in FTAs with developing countries. In addition, the U.S.-Korea FTA (KORUS) does not
place any specific limitations on compulsory licensing.
Parallel Importation. Parallel imports, also known as grey-market goods, refer to goods
imported into a country without permission of the rights-holder after those goods were
legitimately sold elsewhere. Parallel importation relates to the concept of territorial exhaustion of
IPR, which governs the extent of IPR after the first sale. Under a national system of exhaustion
practiced in the United States, IPR are exhausted domestically after the first sale, but not abroad,
thus prohibiting trade in those goods without permission of the rights-holder. Under an
international system, IPR are exhausted at the first sale for any destination, and such goods can be
exported freely. Article 6 of the TRIPS specifically excludes issues arising from exhaustion of
IPR from WTO dispute settlement, allowing each member to adopt different exhaustion regimes.
Thus, TRIPS does not address the issue of parallel imports. Some developing countries contend
that parallel importation is an alternative method for governments to increase access to medicines
in the absence of a compulsory license.65 Pharmaceutical companies have voiced concerns that
this practice threatens their ability to engage in price differentiation between different markets.
U.S. FTAs negotiated with Australia, Singapore, and Morocco disallow parallel importing of
patented products. Subsequent U.S. negotiated FTAs have not included this provision, due to
language included in the Science, State, Justice, and Commerce, and Related Agencies,
Appropriations Act of 2006 (P.L. 109-108), which prohibited the use of such provisions.
64
For example, under the Peru FTA, if a company files to market a new drug in Peru after making an initial filing in
another country, such as the United States, and Peru approves the drug within six months of the filing, the data
exclusivity period begins at the time the drug was approved in the country of the initial filing, not Peru.
65
U.S. Government Accountability Office, U.S. Trade Policy Guidance on WTO Declaration on Access to Medicines
May Need Clarification, GAO-97-1198, September 2007, p. 19.
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Biodiversity and Traditional Knowledge
International trade negotiations increasingly have focused on the protection of plant and animal inventions, new plant
varieties, traditional knowledge, and folklore. Some indigenous communities in developing countries and international
non-governmental organizations have expressed concern about the use of patents to provide private rights for
traditional knowledge and genetic material; the commercial use of such resources by entities other than the
indigenous communities or countries from which such resources are derived; and the distribution of benefits from
commercial use. The United States, other advanced countries, and business groups favor treating traditional
knowledge and genetic material as intellectual property and protecting these resources through an IPR framework.
Article 27.3(b) of the TRIPS Agreement permits Member states to exempt “plants and animals other than microorganisms, and essentially biological processes” from patentability. TRIPS requires Members to protect plant varieties
through patent protection, some other system (“sui generis”), or a combination of the two. Paragraph 19 of the Doha
Declaration added another dimension to the issue by requiring the TRIPS Council to probe the relationship between
the TRIPS Agreement, the UN Convention on Biological Diversity (CBD), and traditional knowledge and folklore.
These issues also are being discussed in WIPO’s Intergovernmental Committee on Intellectual Property and Genetic
Resources, Traditional Knowledge, and Folklore (IGC).
India, Brazil, and Peru, among other countries, contend that patent applicants should be required to disclose the
source of genetic materials, including plant life and traditional knowledge, before obtaining patents. The United States
and the European Union have advocated for national systems in which companies are granted permission to research
genetic materials and are obligated to share benefits from patents derived from those genetic products.
Some earlier U.S. FTAs have required signatories to provide protection for plants, animals, and plant varieties. The
recent FTAs with Peru, Panama, and Colombia do not mandate patentability for plants and animals, but state that the
countries should take efforts to expand patent coverage to these areas and to maintain this protection once it is
offered. Side-letters in the three FTAs state the signatories’ recognition of the importance of biodiversity and
traditional knowledge and pledge the countries to work together to address these issues through the IGC.
Copyright
In the area of copyright protection, the United States has pursued certain TRIPS-plus measures in
FTAs, such as extending copyright terms; including anti-circumvention provisions; and protecting
rights-management information in its FTAs. The TRIPS Agreement does not mention any
57
U.S. Government Accountability Office, U.S. Trade Policy Guidance on WTO Declaration on Access to Medicines
May Need Clarification, GAO-97-1198, September 2007, p. 19.
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obligations regarding rights-management information, which is “electronic information that
identifies a protected work, its author, and terms and conditions of use,”5866 perhaps due to the fact
these technologies were not available at the time. In contrast, U.S.-negotiated trade agreements
prohibit the removal or alteration of such information.
While patent protection has experienced policy shifts in the FTAs with Peru, Panama, and
Colombia, copyright protection provisions have remained fairly consistent through the FTAs. In
general, FTA signatories are obligated to provide an additional twenty years of copyright
protection. This brings the minimum copyright term to seventy years from the death of the author
or authorized publication, compared to fifty under the TRIPS Agreement. Responding to
technological innovations not discussed in the TRIPS Agreement, many of the FTAs require
trading partners to outlaw circumvention of technological measures protecting access to
copyrighted works. These provisions build on the
U.S. Digital Millennium Copyright Act
(DMCA) of 1998.5967 Also based on the DMCA, many
FTAs contain provisions that regulate the
liability of Internet service providers (ISPs) for
copyright infringement that occurs within their networks. Under the FTAs, ISPs are provided
limited immunity from copyright liability in certain kinds of infringing activities if they comply
with regulations. For instance, ISPs must block access to or remove infringing materials as soon
as they are aware of the infringement. Copyright holders argue that it is necessary for ISPs to
assist in enforcing copyright for copyright laws to be effective. However, critics claim that these
provisions impose excessive burdens on ISPs, reduce the rights of internet users, and limit the
policy flexibility of FTA signatories in determining their own IPR regimes.
Table 4. Patent and Copyright Provisions in the TRIPS Agreement and U.S. FTAs
Intellectual
Property
Forms
TRIPS Provisions
General TRIPS-Plus
Provisions in FTAs
Scale-down of TRIPS-Plus
Standards
Mandatory extensions in cases
of unreasonable delays in patent
grants/regulatory approval
Optional extensions in cases
of unreasonable delays in
patent grants/regulatory
approval
Patents
Patent term
extensions
No provisions
Jordan (Article 4.23.a),
Chile (Article 17.9.6; 17.9.2a),
Singapore (Article 16.7.7;
18.8.4a), Australia (Article 17.9.8;
17.10.4), Morocco (Article 15.9.7;
15.10.3), CAFTA-DR (Article
15.9.6; 15.10.2), Bahrain (Article
14.8.6),Oman (Article 15.8.6),
Korea (Article 18.8.6)
Market approval
linked to patent
status
No provisions
NAFTA (no mention),
Jordan (no linkage, but patent
National regulatory authorities
cannot provide marketing
approval for a generic version of
a patented drug without
NAFTA (Article 1709.12)
Peru (Article 16.9.6), Panama
(Article 16.9.6), Colombia
(Article 16.9.6)
Eliminates mandate that
regulatory authorities cannot
approve a generic drug for
marketing if patent for drug
58
CRS Report RL33205, Intellectual Property and the Free Trade Agreements: Innovation Policy Issues, by John R.
Thomas.
59
The DMCA (P.L. 105-304) prohibits disabling technological protection measures designed to protect copyright
works through activities such as descrambling or decrypting copyrighted workers.
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Intellectual
Property
Forms
Protection for
undisclosed test
or other data
TRIPS Provisions
General TRIPS-Plus
Provisions in FTAs
owner must be notified if
another entity is seeking
marketing approval for generic
version of patented product,
Article 4.23.b)
permission from rights-holder;
also requires notification of
rights-holder if marketing
permitted
Members must protect data
from unfair commercial use
(Article 39.3)
Provides for at least five years
of data exclusivity from date of
approval in country for
pharmaceuticals that contain
new chemical products
Jordan (Article 4.22)
Chile (Article 17.10.2b), Singapore
(16.8.4c),Australia (Article
17.10.4), Morocco (Article
15.10.4), CAFTA-DR (Article
15.10.2), Bahrain (Article 14.9.4),
Oman (15.9.4), Korea (Article
18.9.5)
NAFTA (Article 1711.6), Bahrain
(Article 14.9.1), Oman (Article
15.9(1-2), CAFTA-DR (Article
15.10.1), Singapore (Article
16.8(1-3)), Australia (Article
17.10.1), Morocco (Article
15.10.1), Chile (Article 17.10.1),
Korea (Article 18.9(1-2))
Issuance of
compulsory
licenses
Some restrictions in issuance
of compulsory licenses;
circumstances under which
licenses can be issued not
limited (Article 13)
NAFTA (Article 1709.10),
Limits issuance of compulsory
license to specific cases:
Correcting anti-competitive
practices, public noncommercial contexts, national
emergencies, and other
extremely urgent situations
Jordan (Article 4.20), Singapore
(Article 16.7.6), Australia (Article
17.9.7)
Parallel
importing of
patented
products
TRIPS will not be used to
discuss IPR exhaustion
(Article 6)
Biodiversity and
traditional
knowledge
Members may exclude plants
and animals from
patentability (microorganisms and non-biological
and micro-biological
processes must be eligible
for patents); must provide
protection of plant varieties
(Article 27.3(b))
Jordan (no mention), Chile (no
mention), CAFTA-DR (no
mention), Bahrain (no
mention), Oman (no mention)
NAFTA (Article 1709.3),
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Parallel importation can be
restricted or prohibited
NAFTA (Article 1709.5, 1709.9),
Singapore (Article 16.7.2),
Morocco (Article 15.9.4), Australia
(Article 17.9.4)
Countries shall make patents
available for plants and animals
Morocco (Article 15.9.2, plants
and animals mentioned, plant
varieties are not mentioned)
Scale-down of TRIPS-Plus
Standards
in place
Peru (Article 16.10.4), Panama
(Article 15.10.4), Colombia
(Article 16.10.4)
Provides for at least five
years of marketing exclusivity
from date of approval in
country of first filing if new
drug is granted marketing
approval within six months in
country of second filing
Peru (Article 16.10.2), Panama
(Article 15.10.4), Colombia
(Article 16.10.2)
Not discussed
Chile (no mention), Morocco
(no mention), CAFTA-DR (no
mention), Bahrain (no mention),
Oman (no mention)
Peru (no mention), Panama (no
mention), Colombia (no
mention), (no mention)
Not discussed
Peru (no mention), Panama (no
mention), Colombia (no
mention), Korea (no mention)
Members may exclude plants
and animals from
patentability, but shall take
reasonable effort to provide
patent protection for plants
or animals and maintain
protection once offered
Chile (Article 17.9.2, mentions
plants but not animals), CAFTADR (Article 15.9.2), Peru
30
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Intellectual
Property
Forms
TRIPS Provisions
Bahrain (Article 14.8.(1-2)),
Oman (Article 15.8.2, plants
not discussed),
General TRIPS-Plus
Provisions in FTAs
Scale-down of TRIPS-Plus
Standards
(Article 16.9.2), Panama (Article
15.9.2), Colombia (Article
16.9.2)
Jordan, (no mention),
Singapore (no mention),
Australia (no mention), Korea
(no mention)
Copyrights
Rightsmanagement
information
Not discussed
Outlaws removal or alternation of information
NAFTA (no mention), Jordan
(no mention)
Chile (Article 17.5.6), Australia (Article 17.4.8), Singapore (Article
16.4.8), Morocco (Article 15.5.9), CAFTA-DR (Article 15.5.8), Bahrain
(Article 14.4.8), Oman (Article 15.4.8), Peru (Article 16.7.5), Panama
(Article 15.5.8), Colombia (Article 16.7.5), Korea (Article 18.4.8)
Term of
protection
No less than 50 years from
authorized publication
(Article 12)
No less than 70 years from death of author or authorized
publication
NAFTA (Article 1705.4), Jordan
(no mention)
Chile (Article 17.5.4), Singapore (Article 16.4.4), Australia (Article
17.4.4), Morocco (Article 15.5.5), CAFTA-DR (Article 15.5.4), Bahrain
(Article 14.4.4), Oman (Article 15.4.4), Peru (Article 16.5.5), Panama
(Article 15.5.4), Colombia (Article 16.5.5), Korea (Article 18.4.4)
Circumvention
of copyrighted
work
Not discussed
Signatories must agree to prohibit circumvention
NAFTA (no mention)
Jordan (Article 4.6), Chile (Article 17.5.5), Singapore (Article 16.4.7),
Australia (Article 17.4.7), Morocco (Article 15.5.8), CAFTA-DR (Article
15.5.7), Bahrain (Article 14.4.7), Oman (Article 15.4.7), Peru (Article
16.7.4), Panama (Article 15.5.7), Colombia (Article 16.7.4), Korea
(Article 18.4.7)
ISP Liability
Not discussed
ISPs are provided with limited liability in certain situations of
copyright infringement on their servers if they comply with
regulations
NAFTA (no mention), Jordan
(no mention)
Chile (Article 17.11.23), Singapore (Article 16.9.22), Australia (Article
17.11.29), Morocco, CAFTA-DR (Article 15.11.27), Bahrain, Oman
(Article 15.10.29), Peru (Article 16.11.29), Panama (Article 15.11.27),
Colombia (Article 16.11.29), Korea (Article 18.10.30)
Note: When there is no mention of an issue in an FTA, the TRIPS standard generally holds.
U.S. Trade Law
Special 301
Section 301 of the Trade Act of 1974 (P.L. 93-618), as amended, is the principle U.S. statute for
identifying foreign trade barriers due to inadequate intellectual property protection. The 1988
Omnibus Trade and Competitiveness Act (P.L. 100-418) strengthened section 301 by creating
“Special 301” provisions, which require the USTR to conduct an annual review of foreign
countries’ intellectual property policies and practices. By April 30th of each year, the USTR must
identify countries that do not offer “adequate and effective” protection of IPR or “fair and
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equitable market access to United States person that rely upon intellectual property rights.”
According to an amendment to the Special 301 provisions by the Uruguay Round Agreements Act
(P.L. 103-465), the USTR can identify a country as denying sufficient intellectual property
protection even if the country is complying with its TRIPS commitments. These findings are
submitted in the USTR’s annual “Special 301” report.
Special 301 Country Lists
Within 30 days of submitting the annual National Trade Estimates of Foreign Trade Barriers
report, the USTR must determine which of the identified countries are “Priority Foreign
Countries.” Countries that “have the most onerous or egregious acts, policies or practices that
deny intellectual property protection and limit market access to U.S. persons or firms depending
on intellectual property rights protection” and “have the greatest adverse impact (actual or
potential) on the relevant United States products” may be identified as “Priority Foreign
Countries.” These countries may be investigated under section 301 provisions of the Trade Act of
1974. The USTR cannot identify countries as Priority Foreign Countries if they have entered into
good faith negotiations or have made significant progress in improving their intellectual property
protection record. 60
If a country is named as a “Priority Foreign Country,” the USTR must launch an investigation
into that country’s IPR practices. This investigation is conducted in a manner similar to a “Section
301” investigation; the USTR must determine a course of action within six months (9 months if a
determination of complex circumstances is made). The USTR may suspend trade concessions and
impose import restrictions or duties, or enter into a binding agreement with the priority country
that would eliminate the act, policy, or practice that is the subject of the action to be taken. Since
the advent of the WTO and its recourse to dispute settlement, the use of the first option may lead
to the initiation of dispute settlement proceedings at the WTO for member countries, rather than
unilateral retaliation. For countries outside the WTO, the possibility of trade sanctions remain.
The USTR also has created several administrative categories for country identification in the
Special 301 Report. “Priority Watch List” countries are those whose acts, policies, and practices
warrant concern, but do not meet all of the criteria for identification as a Priority Foreign Country.
The USTR may place a country on the Priority Watch List when the country lacks proper
intellectual property protection and has a market of significant U.S. interest. “Watch List”
countries have intellectual property protection inadequacies that are less severe than those on the
Priority Watch List, but still attract U.S. attention. Just being on one of the Special 301 lists may
induce countries to improve their IPR protection. Finally, countries identified for “Section 306”
are monitored for compliance with bilateral intellectual property agreements used to resolve
investigations under section 301. Additionally, the USTR launches out-of-cycle reviews (OCRs)
on countries to monitor their progress on intellectual property issues. OCRs are conducted on
countries that USTR considers to require further review and may result in status changes for the
following year’s Special 301 report.
60
For the Special 301 provisions, see 19 U.S.C. §2242; Trade Act of 1974, as amended, (P.L. 93-618), §182.
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Special 301 Report for 2010
For the 2010 Special 301 Report, the USTR reviewed the IPR policies and practices of 77 countries. 61
•
Despite some improvements, China and Russia remain top concerns for the Administration due to their
inadequate IPR regimes.
•
The USTR placed eleven countries on the Priority Watch List: Algeria, Argentina, Canada, Chile, China, India,
Indonesia, Pakistan, Russia, Thailand, and Venezuela.
•
The USTR placed another 29 countries were placed on the Watch List.
•
No countries were designated as Priority Foreign Countries. Paraguay was identified for Section 306 monitoring.
•
The USTR announced that it would conduct OCRs for the Philippines and Thailand to monitor these nations’
progress on IPR and to evaluate their Special 301 status.
•
Israel’s status in the Special 301 Report is pending, following the conclusion of an OCR and an understanding
reached by the United States and Israel on several issues in Israel’s IPR regime for pharmaceutical products.62
•
The USTR removed the Czech Republic, Hungary, and Poland from the Special 301Watch List for significant
improvement in their protection and enforcement of IPR. Following an OCR on Saudi Arabia, the USTR decided
to remove Saudi Arabia from the Watch List on the basis of improvements in IPR enforcement, prosecution, and
transparency issues.
Country Identification Factors
Identification of countries for the “Special 301” lists is a lengthy process of information gathering
and analysis based on the USTR’s annual trade barriers report and consultations with a wide
variety of sources, including government agencies, industry groups, other private sector
representatives, Congressional leaders, and foreign governments. The Special 301 statute is the
overall guideline for identifying countries for the various lists. However, placements are countryspecific and, according to a USTR official, take into consideration a host of factors, several of
which are mentioned in the Special 301 report.63 These include the level and scope of the
country’s IPR infringement and their impact on the U.S. economy. Other considerations include
the strength of the country’s IPR laws and enforcement of IPR laws. The USTR also evaluates
progress made by the country in improving IPR protection and enforcement in the past year.
However, even significant progress oftentimes does not change the position or inclusion of a
country on the lists. For instance, the USTR may decide not to upgrade a country from the
Priority Watch List to the Watch List so that it can continue monitoring the country’s intellectual
property practices. Also, the USTR may note significant progress made by a country but not
remove the country from the Special 301 list in order to continue highlighting concerns about the
country’s practices and limit backsliding. Another consideration for the USTR is the sincerity of
the country’s commitment to multilateral and bilateral trade agreements. There is no weighting
criteria for the factors or a formula to determine the placement of a country on the watch list.
Furthermore, no particular threshold exists for determining when a country should be upgraded or
downgraded on the list.
61
The USTR Special 301 Report 2010 is available on the USTR website, http://www.ustr.gov.
62
Letter from Ambassador Ron Kirk, U.S. Trade Representative, to The Honorable Benyamin Ben-Eliezer, Ministry of
Industry, Trade and Labor, February 18, 2010.
63
Conversation with USTR official, July 2006.
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Some observers speculate that the Special 301 rankings are subject to external influences. The
lack of a specific framework for placing countries, aside from the general directives from the
Special 301 statute, has raised concerns that foreign policy considerations affect the process. For
example, an IIPA representative suggested that USTR placement of countries is influenced by
geopolitical reasons. 64 This source cites Russia as an example of a country with high IPR
infringement that could be named as a Priority Foreign Country but is not due to unrelated foreign
policy considerations. Other observers of U.S. trade policy suggest that pharmaceutical
companies have a stronghold on policy direction. Oxfam International, a confederation of
poverty-alleviation organizations, contends that the U.S. government’s policy on patents “is still
largely influenced by the narrow commercial interests of the giant pharmaceutical companies.”65
A USTR official stated that the interests of pharmaceutical companies do not override concerns
by other interest groups in evaluating country placement for the Special 301 report. The official
emphasized that all industry group submissions are given fair and due consideration.66
Section 337
Section 337 of the Tariff Act of 1930 (19 U.S.C. 1337), as amended, prohibits unfair methods of
competition or other unfair acts in the importation of products into the United States. It also
prohibits the importation of articles that infringe valid U.S. patents, copyrights, processes,
trademarks, semiconductor products produced by infringing a protected mask work, or protected
design rights. While the statute has been utilized to counter imports of products judged to be
produced by unfair competition, monopolistic, or anti-competitive practices, it has become
increasingly used for its IPR enforcement functions in recent years. Under the statute, the import
or sale of an infringing product is illegal only if a U.S. industry is producing an article covered by
the relevant IPR exists or is in the process of being established. However, unlike other trade
remedies such as antidumping or countervailing duty actions, no showing of injury due to the
import is required.
The U.S. International Trade Commission (ITC) administers section 337 proceedings. USITC
must investigate complaints either brought to it or ones commenced under its own initiative. An
administrative law judge (ALJ) provides an initial determination (ID) to the ITC which can accept
the ID or order a further review of it in whole or in part. If the ITC finds a violation, it may issue
two types of remedies: exclusion orders or cease and desist orders. The ITC may issue either a
limited or general exclusion order enforced by U.S. Customs. A general exclusion order directs
U.S. Customs to keep out all infringing articles regardless of the source. More commonly, a
limited exclusion order is employed to exclude infringing articles from the firm subject to the
ITC’s investigation. Alternatively, the ITC may enforce a cease and desist order to stop the sale of
the infringing product in the United States. However, the ITC may consider several public interest
criteria and decline to issue a remedy. Also, the President may disapprove a remedial order during
a 60 day period for “policy reasons,” which has been interpreted to mean national security
reasons.67
64
Telephone conversation with PhRMA representative, July 2006.
Oxfam International, US bullying on drug patents: One year after Doha, Briefing Paper 33.
66
Telephone conversation with USTR official, July 2006.
67
For more information on the Section 337 investigation and enforcement process, see CRS Report RS22880,
Intellectual Property Rights Protection and Enforcement: Section 337 of the Tariff Act of 1930, by Shayerah Ilias.
65
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During FY2009, the ITC reported a total of 85 active section 337 investigations and ancillary
proceedings, comparable to the FY2008 level. Of the 85 active investigations in FY2009, 29
constituted of new section 337 investigations and 7 were new ancillary proceedings stemming
from previously concluded section 337 investigations. The section 337 investigations frequently
involved advanced technology areas, such as integrated circuit, computer, telecommunications,
and other electronic technologies. Over 60% of the new section 337 investigations that were
active in FY2009 involved cases of alleged patent infringement. In FY2009, the ITC issued three
general exclusion orders, eight limited exclusion orders, and 23 cease-and-desist orders.68
Generalized System of Preferences
The Generalized System of Preferences (GSP) is a program that provides preferential duty-free
entry to certain products from designated developing countries. The purpose of the program is to
foster economic growth in developing countries by increasing their export markets. The Trade Act
of 1974 authorized the GSP for a ten-year time frame, and the program has been renewed from
time to time. Most recently, in 2006, Congress extended GSP through December 31, 2010.69
Although the GSP is non-reciprocal, it can be used to promote stronger intellectual property
protection and enforcement abroad. Under the GSP statute, the President must consider a set of
mandatory criteria that a country must fulfill in order to be designated as a GSP beneficiary.
Additionally, the President may evaluate a country on the basis of certain discretionary criteria,
including the country’s provision of IPR protection.70
The GSP program undergoes an annual review by the GSP Subcommittee of the Trade Policy
Staff Committee (TPSC), which is headed by the USTR. As part of its evaluation, the TPSC
addresses concerns about specific country practices (such as intellectual property protection) and
makes recommendations to the President. For 2009, the USTR continued to evaluate IPR
protection in Lebanon, Russia, and Uzbekistan on the basis of IIPA petitions for ongoing GSP
reviews.71
U.S. Agency Functions and Funding for IPR
The United States has a complex apparatus for supporting intellectual property rights, with
responsibilities cutting across many different federal government agencies. Protection activities
include developing IPR policy, informing and advising Congress about IPR-related issues,
participating in international trade negotiations to promote IPR, and providing IPR training and
technical assistance in other countries. Enforcement activities involve the conduct of criminal
investigations in the United States and abroad, interdiction of pirated and counterfeit goods, and
monitoring of compliance with trade agreements. Enforcement also involves capacity-building
activities to foster stronger IPR law enforcement in other countries.
68
U.S. International Trade Commission, Year in Review: Fiscal Year 2009, USITC Publication 4167, p. 14.
For a more thorough discussion of GSP, see CRS Report RL33663, Generalized System of Preferences: Background
and Renewal Debate, by Vivian C. Jones.
70
91 USC 2462(b)(2)
71
USTR, GSP: 2009 Annual Review, http://www.ustr.gov.
69
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It is difficult to obtain a complete picture of the magnitude of federal budget devoted to
intellectual property laws. Some of these agencies perform their IPR related activities within
existing budget parameters, and do not differentiate specific sums devoted to IPR-related
activities. What follows is a discussion of the various IPR functions of U.S. agencies.
Department of Commerce (Commerce)
Two agencies within the Department of Commerce, the Patent and Trademark Office (PTO) and
the International Trade Administration (ITA), address IPR issues.72
United States Patent and Trademark Office (PTO)
The PTO administers the U.S. laws pertaining to patents and trademarks. The agency processes
patent and trademark applications, issues patents and registers trademarks, and circulates patent
and trademark information. The PTO develops IPR protection and enforcement policy and
collaborates with other agencies to develop intellectual property provisions in FTAs and other
international agreements. Additionally, the PTO offers training, technical assistance, and trade
capacity building programs to assist in promoting strong IPR regimes in foreign countries.73 The
PTO does not have jurisdiction over determining patent and trademark infringements; such
determinations and remedies are made at the U.S. federal district court level or through the U.S.
International Trade Commission’s section 337 proceedings (discussed above). 74 The PTO is fully
funded through fees generated from patent and trademark applications. The Consolidated
Appropriations Act, 2010 (P.L. 111-117) provided $1.89 billion in budgetary authority to the PTO
for FY2010, down from $2.01 billion provided for FY2009 (P.L. 111-8).
International Trade Administration (ITA)
The ITA administers many of the international trade programs of the Department of Commerce,
include aspects involving IPR. The ITA monitors foreign countries’ progress in implementing
intellectual property agreements; reviews Generalized System of Preferences (GSP) petitions
submitted by industry and coordinates the Commerce Department’s response to these petitions;
represents the Commerce Department at the WTO TRIPS Council; meets with trading partners to
advance U.S. intellectual property interests abroad; and works with U.S. businesses and industry
groups to make sure that IPR-related trade concerns are addressed. 75 For FY2010, the
Consolidated Appropriations Act, 2010 (P.L. 111-117) provided the ITA with $456.20 million
(including both direct appropriation and anticipated receipts from fees), up from $429.9 million
provided in FY2009 (P.L. 111-8).
72
General information about the Department of Commerce is available at http://www.doc.gov.
NIPLECC, Report to the President and Congress on Coordination of Intellectual Property Enforcement and
Protection, January 2008, p. 21.
74
Conversation with PTO official, November 26, 2007.
75
NIPLECC, Report to the President and Congress on Coordination of Intellectual Property Enforcement and
Protection, January 2008, p. 21.
73
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Department of Justice (DOJ)
The DOJ enforces criminal laws that protect IPR in the United States and internationally through
the prosecution of intellectual property cases. The Civil Division’s Office of Consumer Litigation
specializes in intellectual property cases involving public health and safety. The Federal Bureau
of Investigation (FBI) has an intellectual property enforcement program focusing on those
intellectual property crimes that have the most bearing on national and economic security, such as
trade secret theft, Internet piracy, and counterfeit good trafficking.76 In addition to enforcement
activities, the DOJ also works with Congress to develop laws that increase protection of IPR and
provides training and technical assistance programs on IPR enforcement through its Criminal
Division. The Consolidated Appropriations Act, 2010 (P.L. 111-117) provided $7.66 billion to the
FBI for FY2010, up from the FY2009 level of $7.07 billion (P.L. 111-8).
Department of Homeland Security (DHS)
The DHS, through its Customs and Border Protection (CPB) unit and Immigration and Customs
Enforcement (ICE) unit, conducts intellectual property rights enforcement activities. Neither DHS
unit has a line item for IPR enforcement. The ICE and the FBI jointly run the National
Intellectual Property Rights Coordination Center that coordinates U.S. Government domestic and
international law enforcement activities.77
Customs and Border Protection (CBP)
Taking the lead in day-to-day IPR enforcement activities at the U.S. border, the CBP is
responsible for detecting and seizing counterfeit and pirated goods entering the United States and
determining penalties for infringement.78 CBP has the authority to determine whether or not
imports infringe federally registered trademarks and copyrights and to detain or seize such
infringing goods. Owners of copyrights and trademarks are able to record information about their
rights in the CBP’s electronic IPR database. As noted earlier, in contrast to trademarks and
copyrights, CBP does not have the jurisdiction to make determinations about patent
infringements. However, it is able to block imports determined by the ITC to infringe a U.S.
patent by a Section 337 investigation. 79 For FY2010, the Consolidated Appropriations Act, 2010
provided $8.07 billion in budget authority to CBP, up from $7.60 billion in FY2009.
Immigration and Customs Enforcement (ICE)
ICE is charged with investigating violations of U.S. law that are connected with U.S. borders.
ICE “identifies, investigates, apprehends, and removes” international criminal groups and other
criminals. ICE conducts inquiries into the importation and distribution of counterfeit goods. ICE
activities are closely linked with those of CBP. For instance, when CBP identifies and seizes
counterfeit goods, the issue is referred to ICE for criminal investigation. Likewise, information
76
DOJ, Progress Report of the Department of Justice’s Task Force on Intellectual Property, June 2006,
http://www.usdoj.gov/opa/documents/ipreport61906.pdf, pp. 17-24.
77
Information about the DHS is available at http://www.dhs.gov.
78
Certain customs-related IPR policy-making resides within the Treasury.
79
NIPLECC, Report to the President and Congress on Coordination of Intellectual Property Enforcement and
Protection, January 2008, pp. 15-16. Additional information about CBP is available at http://www.cbp.gov.
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obtained from ICE activities that is relevant to identifying and apprehending counterfeit
shipments is provided to CBP.80 For FY2010, the Consolidated Appropriations Act, 2010
provided $5.34 billion in budget authority to ICE, up from $4.93 billion in FY2009.
Food and Drug Administration (FDA)
The FDA, which is an agency of the Department of Health and Human Services (DHHS), is
responsible for protecting public health by ensuring the safety and effectiveness of medicines,
food, and other products. As part of its activities, the FDA works to protect consumers against
counterfeit medicines. To combat the entry of foreign counterfeit drugs into the U.S. drug supply,
the FDA works in conjunction with the CBP to conduct border inspections of FDA-regulated
products. The FDA also engages in foreign inspections to ensure that foreign manufacturers meet
FDA quality and labeling requirements. Funding for preventing counterfeits from entering the
United States is part of overall FDA import safety efforts.81 The enacted FY2010 Agricultural
appropriation, P.L. 111-80, contained $2.36 billion in budget authority for the FDA, up from
$2.05 billion for FY2009.
Copyright Office
The Copyright Office of the Library of Congress administers U.S. copyright law by registering
claims to copyright and related documents, including “assignments or transfers of rights” and
maintains information on registrations, recordings, compulsory licenses, and other copyrightrelated actions. Additionally, the Copyright Office provides legal and technical expertise on
national and international copyright issues to the U.S. government. The Copyright Office also
works with other federal agencies to provide assistance and advice in negotiations for
international intellectual property agreements, as well as technical assistance to foreign countries
crafting their own copyright laws.82 The enacted FY2010 Legislative appropriation, P.L. 111-68,
contained $20.9 million in new budget authority (not including authority to spend $33.3 million
in receipts) for the Copyright Office, up from $18.3 million in new budget authority in FY2009
(not including authority to spend $33.3 million receipts).
Copyright Office appropriations also specify funding for IPR-related activities in developing
countries. As in previous years, the FY2010 appropriations act provided $100,000 to the
International Copyright Institute for such activities.
Department of State (State)
State represents U.S. views in both bilateral and multilateral arenas. State works to build
international consensus for intellectual property rights enforcement. Information from State’s
foreign postings informs the USTR Special 301 review. In particular, the Bureau of International
Narcotics Control and Law Enforcement (INCLE) works to combat intellectual property piracy,
while the Bureau of Energy, Economics and Business Affairs supports stronger international IPR
80
Ibid. Also refer to the ICE website, http://www.ice.gov.
81
Conversation with FDA official, November 26, 2007. Additional information is available on the FDA website,
http://www.fda.gov.
82
NIPLECC, Report to the President and Congress on Coordination of Intellectual Property Enforcement and
Protection, January 2008, p. 18. Also see Copyright Office website, http://www.copyright.gov.
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standards to fight global piracy and counterfeiting. 83 As in previous years, the Consolidated
Appropriations Act, 2010 (P.L. 111-117) provided $5 million from the INCLE Account for
combating copyright piracy (Section 688).
U.S. Agency for International Development (AID)
AID funds training and technical assistance to improve the compliance with the TRIPS
Agreement and bilateral trade agreements with the United States. Funding for these projects
generally have been undertaken by regional or country missions; there is no separate budgetary
line item for IPR enforcement and training. 84
United States Trade Representative (USTR)
The USTR is the lead trade agency of the United States government. Through its annual Special
301 report, USTR is charged with monitoring the adequacy and effectiveness of IPR protection of
our trading partners as well as their compliance with bilateral and multilateral trade agreements,
to identify countries not in compliance with such agreements, and to negotiate with those
countries better compliance. USTR also advances greater protection and enforcement of IPR in its
negotiations of U.S. free trade agreements. Additionally, USTR works to implement the
Administration’s STOP! Initiative, which draws together the major federal government agencies,
private sector groups, and trading partners to take targeted action in fighting piracy and
counterfeiting.85 The FY2010 funding level for USTR was $47.83 million, under the
Consolidated Appropriations Act, 2010 (P.L. 111-117), up from the FY2009 funding level of
$47.3 million. Explanatory language in H.Rept. 111-149, accompanying P.L. 111-117, encouraged
the USTR to continue prioritizing IPR issues with China, Russia, and Canada in bilateral and
multilateral trade negotiations.
United States International Trade Commission (ITC)
The ITC is a quasi-judicial federal government agency responsible for investigating and
arbitrating complaints of unfair trade practices. The ITC adjudicates allegations of imported
products that infringe U.S. patents, trademarks, and copyrights through its section 337
proceedings (see above). The primary remedy employed by the ITC is to order the CBP to stop
imports from entering the border. Additionally, the ITC may issue “cease and desist” orders
against individuals determined to be IPR violators. Damages for IPR infringement cannot be
received through ITC court proceedings; rights-holders seeking damages must file action with the
U.S. federal district court.86 For FY2010, the Consolidated Appropriations Act, 2010 (P.L. 111117) provided the ITC with $81.86 million in budget authority, up from the FY2009 level of
$75.1 million.
83
NIPLECC, Report to the President and Congress on Coordination of Intellectual Property Enforcement and
Protection, January 2008, pp. 17-18. Additional information about the State Department is available at
http://www.state.gov.
84
Trade Capacity Database and general AID information is accessible at http://www.usaid.gov.
85
NIPLECC, Report to the President and Congress on Coordination of Intellectual Property Enforcement and
Protection, January 2008, p. 25. Also see USTR website, http://www.ustr.gov.
86
U.S. ITC website, http://www.usitc.gov.
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Intellectual Property Enforcement Coordinator (IPEC)
In October 2008, Congress created an Intellectual Property Enforcement Coordinator (IPEC),
through the Prioritizing Resources and Organization for Intellectual Property Act of 2008 (P.L.
110-403). The IPEC, located in the Executive Office of the President – specifically in the Office
of Management and Budget – and subject to Senate confirmation, is charged with coordinating
U.S. government agency IPR enforcement actions and with providing assistance to the USTR in
conducting trade negotiations relating to IPR enforcement abroad.87
Under P.L. 110-403, the IPEC is to chair a Advisory Committee composed of representatives
from the Office of Management and Budget, the Departments of Justice, Commerce, State,
Homeland Security, Agriculture, the Food and Drug Administration, the Agency for International
Development, and the Register of Copyrights.
The IPEC, assisted by its Advisory Committee, also is charged with developing a “Joint Strategic
Plan” for combating counterfeiting and piracy. Legislation requires the Joint Strategic Plan to
include in its objectives: reducing counterfeiting and infringing goods in the domestic and
international supply chain, identifying and addressing barriers to effective enforcement
domestically, ensuring that information is shared among the relevant departments and agencies,
eliminating domestic and international counterfeiting and infringement networks, strengthening
the capacity of foreign countries to protect and enforce IPR, and cooperating with other countries
to establish international standards and policies to enforce IPR.
In 2009, President Obama nominated and the Senate confirmed Victoria A. Espinel as the IPEC.
In June 2010, IPEC Espinel released the 2010 Joint Strategic Plan on Intellectual Property
Enforcement. The plan identifies 33 “enforcement strategy action items,” categorized under six
major areas of focus: (1) leading by example; (2) increasing transparency; (3) ensuring efficiency
and coordination; (4) enforcing U.S. rights internationally; (5) securing the supply chain; and (6)
building a data-driven government.88
The House Conference Report (H.Rept. 111-366 to H.R. 3288) provided for a transfer of
$176,000 from the White House to the OMB, to reflect the Administration’s decision to locate the
new IPEC in the OMB rather than the White House.
Issues for Congress
The role of Congress in addressing IPR and trade-related issues stems from the U.S. Constitution,
which provides Congress with the power “To promote the Progress of Science and useful Arts, by
securing for limited Times to Authors and Inventors the exclusive Right to their respective
87
In creating the IPEC, P.L. 110-403 repealed the authorities creating the National Intellectual Property Law
Enforcement Coordination Council (NIPLECC). Established by Congress in 1999, NIPLECC coordinated U.S.
activities to protect and enforce IPR domestically and abroad, drawing together the major federal agencies the help to
enforce IPR. The Copyright Office participated in the Council in an advisory role. The U.S. Coordinator for
International Intellectual Property Enforcement headed NIPLECC’s interagency coordination efforts. NIPLECC,
Report to the President and Congress on Coordination of Intellectual Property Enforcement and Protection, January
2008, pp. 3-4.
88
Executive Office of the President, 2010 Joint Strategic Plan on Intellectual Property Enforcement, June 2010,
http://www.whitehouse.gov/sites/default/files/omb/assets/intellectualproperty/intellectualproperty_strategic_plan.pdf.
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Writings and Discoveries” and “To regulate Commerce with foreign Nations.”89 While the U.S.
Constitution provides Congress with the power to regulate international trade, the authority to
negotiate trade agreements has been delegated periodically to the President. However,
congressional action is needed to bring the trade agreements into force.
From a policy perspective, congressional consideration of IPR may take place in the context of
the National Export Initiative (NEI), an Obama Administration plan introduced in early 2010 to
double U.S. exports in five years to create two million U.S. jobs.90 A report submitted by the
President’s Export Promotion Cabinet on implementing the NEI discussed the relationship
between strengthening IPR regimes internationally and promoting U.S. exports.91 In December
2010, the President’s Export Council sent a letter to President Obama highlighting the importance
of addressing inadequate protection and enforcement of IPR as a means for “boosting exports and
foreign sales, and promoting the sustained growth of well compensated U.S. jobs.” The
President’s Export Council expressed support for making “efforts to combat weak and ineffective
intellectual property regimes abroad an integral and essential part of the National Export
Initiative.” 92
U.S. Efforts to Promote IPR Through Trade Policy
Since the inclusion of IPR provisions in the TRIPS Agreement, there has been an ongoing debate
about the appropriateness of including IPR as a component of U.S. trade policy. Some argue that
IPR, which grant legal temporary monopolies to rights-holders for their creations, are actually
barriers to trade and have no place in trade liberalization negotiations. Others contend that IPR
promote trade through innovation, economic growth, and technology transfer from advanced to
developing countries.
In addition to this broader discussion about the role of IPR in trade policy, concerns have been
voiced about the trade policy channels used by the United States to promote international IPR
protection and enforcement. Some question the appropriateness of using regional and bilateral
FTAs for this pursuing stronger IPR, contending that such actions take away from the
effectiveness of multilateral IPR promotion efforts. Periodically, Members of Congress have
expressed concern over U.S attempts to expand the IPR obligations of foreign countries through
trade agreements. In 2002, the Trade Promotion Authority (TPA) legislation was amended to state
that the United States recognized the Doha Declaration on the TRIPS Agreement and Public
Health in the context of negotiating FTAs. In the 110th Congress, congressional leaders and the
Bush Administration agreed to modifications of the patent provisions in the Peru FTA as a result
of the May 2007 bipartisan trade agreement. Still, a Government Accountability Office (GAO)
report suggests that USTR should offer clearer policy guidance to align FTA negotiating activities
89
U.S. Constitution, Article 1, Section 8.
90
“National Export Initiative,” Executive Order 13534 of March 11, 2010, 75 Federal Registrar 12433, March 16,
2010.
91
Export Promotion Cabinet, Report to the President on the National Export Initiative: The Export Promotion
Cabinet's Plan for Doubling U.S. Exports in Five Years, Washington, D.C., September 2010. The President’s Export
Promotion Cabinet is a high-level body comprised of the Secretaries or Directors of key federal agencies involved in
U.S. export promotion efforts.
92
Letter from Jim McNerney, The President's Export Council, to President Obama, December 9, 2010,
http://trade.gov/pec/docs/PEC_IPR_Letter_120910.pdf. The President’s Export Council is a private sector national
advisory committee on international trade.
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with the WTO Doha Declaration.93 Additionally, there is concern by some that the ratchet of IPR
commitments pursued through regional and bilateral FTAs may be too stringent for developing
countries and may limit innovation and creativity by stifling the exchange of ideas.
Further expansion of IPR provisions may be affected by the language of any future TPA. In
discussions about renewal of TPA, Congress may choose to consider possible reiteration or
expansion on its IPR goals related to global health from the 2002 TPA. Congress also may choose
to consider whether or not to follow the template provided by the Peru, Panama, and Colombia
FTAs in future trade negotiations, such as negotiations on the Trans-Pacific Partnership
Agreement.
Effectiveness of the U.S. IPR Organizational Structure
There are concerns on the part of some lawmakers about whether or not the present U.S. IPR
organizational structure is doing enough to enforce foreign countries’ IPR obligations, as well as
concerns about whether or not the structure is capable of doing more.
Prior to the establishment of the Intellectual Property Enforcement Coordinator (IPEC), the U.S.
IPR organizational structure was coordinated by the National Intellectual Property Law
Enforcement Coordinating Council (NIPLECC). Some Members of Congress were critical of
NIPLECC’s organizational response to international IPR protection and enforcement. Recent
GAO testimony pointed out some of the problems associated with NIPLECC, including an
absence of mission, dearth of activities, and poor image among businesses. 94 The FY2007 CJS
Committee Report (S.Rept. 109-280) expressed concern about the lack of information on
NIPLECC’s progress and evidence of success.
In the 110th Congress, several bills were introduced to repeal and replace NIPLECC. The
Prioritizing Resources and Organization for Intellectual Property Act of 2008 (P.L. 110-403) was
signed by President Bush on October 13, 2008. The act, among other provisions, replaced
NIPLECC with an IPEC. Elevating the IPEC’s profile by placing it in the EOP, some lawmakers
hope, will promote more effective coordination of the organizational structure’s response to
international IPR protection and enforcement issues. Others argue that the effectiveness of the
IPEC will depend on what resources are allocated for its activities.
While protection and enforcement of IPR is a stated trade policy priority for the United States, it
is difficult to get a sense of the magnitude of funding and resources devoted toward IPR support.
Some agencies do not have a separate budgetary line item for IPR-related activities, and Congress
does not always designate specific funds for IPR activities in its appropriations for agencies.95
Additionally, there is limited information on the economic and other impacts of piracy and
counterfeiting on the United States. For example, in its Special 301 Report, USTR uses industry
figures that are not independently confirmed. This may complicate the ability of lawmakers to
93
U.S. Government Accountability Office, U.S. Trade Policy Guidance on WTO Declaration on Access to Medicines
May Need Clarification, GAO-07-1198, September 2007.
94
U.S. Government Accountability Office, National Enforcement Strategy Needs Stronger Leadership and More
Accountability, GAO-07-710T, April 12, 2007, pp. 8-10.
95
Liza Porteus Viana, “US Fiscal 2009 Proposed Budget Shows IP Enforcement a Priority,” Intellectual Property
Watch, February 6, 2008.
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weigh the threat of IPR infringement against the federal resources available for IPR and other
government priorities.
Legislation was introduced in the 111th Congress to advance U.S. IPR protection and enforcement
efforts as part of U.S. trade policy. The Trade Enforcement Act of 2009 (H.R. 496, S. 1466)
would have created new IPR coordinator positions in the Department of the Treasury and the
Department of Homeland Security’s Customs and Border Protection (CBP) and Immigration and
Customs Enforcement (ICE) agencies; increased IPR resources, staff, funding, and training for
CBP and ICE; required the development of a strategy for IPR enforcement; and created a
Advisory Committee on Import Safety and Intellectual Property Rights Enforcement, among
other provisions.
Some lawmakers also support increasing the priority that IPR is given as part of U.S. foreign
policy. Foreign relations appropriations legislation for FY2010 ( H.R. 2410, H.R. 2475) would
have required the Secretary of State to appoint ten intellectual property attachés to serve in U.S.
missions overseas and would have directed the Secretary of State to consider assigning such
attachés to missions in countries which have been identified under Section 182 of the Trade Act
of 1974.
Some may support efforts to promote IPR as a part of U.S. trade, foreign, or other forms of
policy. Others may raise concerns about how the promotion of IPR may affect U.S. efforts to
advance other policy goals. In addition, while some support efforts to increase resources
dedicated to IPR protection and enforcement, others question what implications such increased
resources might have for U.S. coordination of IPR protection and enforcement activities.
Author Contact Information
Shayerah Ilias
Analyst in International Trade and Finance
silias@crs.loc.gov, 7-9253
Congressional Research Service
Ian F. Fergusson
Specialist in International Trade and Finance
ifergusson@crs.loc.gov, 7-4997
43
66
CRS Report RL33205, Intellectual Property and the Free Trade Agreements: Innovation Policy Issues, by John R.
Thomas.
67
The DMCA (P.L. 105-304) prohibits disabling technological protection measures designed to protect copyright
works through activities such as descrambling or decrypting copyrighted works.
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networks. Under the FTAs, ISPs are provided limited immunity from copyright liability in certain
kinds of infringing activities if they comply with regulations. For instance, ISPs must block
access to or remove infringing materials as soon as they are aware of the infringement. Copyright
holders argue that it is necessary for ISPs to assist in enforcing copyright for copyright laws to be
effective. However, critics claim that these provisions impose excessive burdens on ISPs, reduce
the rights of Internet users, and limit the policy flexibility of FTA signatories in determining their
own IPR regimes.
Trade Secrets
A company’s ability to protect its commercially valuable proprietary information may affect its
competitiveness or even its survival. Such proprietary information can include blueprints,
production processes, marketing strategies, or sales information. In its 2013 Special 301 Report
(discussed below), USTR described the protection of U.S. trade secrets as a growing challenge
threatening the economic security of the United States. The report responded to concerns of U.S.
business that governments have pressured them to reveal trade secrets or to transfer technology to
further a country’s ‘indigenous innovation’ policies. Companies are also reportedly increasingly
victimized by outright theft of their trade secrets, and have decried the often lax remedies
available to combat such theft. Trade secret theft has taken on new and increased complexities in
the digital environment, and the United States is increasingly concerned about trade secret theft
through cybercrime. Penalties for trade secret theft vary widely among countries; some countries
have no penalties at all while others have civil remedies or criminalize trade secret theft that
results from computer hacking. In the United States, remedies for trade secret theft primarily are
found in state law.68
While the U.S. aim in the intellectual property chapters of the TPP seeks to establish criminal
penalties for the theft of trade secrets, it may pursue aspects of this agenda through other trade
negotiations or means of economic statecraft. Such an agenda may involve prohibiting countries
from: (1) conditioning market access on technology transfer; (2) seeking concessional terms for
acquiring or licensing IPR by state-owned enterprises (SOEs); (3) requiring the use of locally
owned or developed IPR; (4) promoting the development of local standards to unfairly advantage
local firms; and (5) requiring the unnecessary disclosure of confidential business information, or
failing to protect such information. The Obama Administration’s strategy on mitigating the theft
of U.S. trade secrets, released in February 2013, underscores U.S. interest in seeking, in U.S.
trade negotiations, new criminal remedy provisions for trade secret theft—similar to remedies
provided in U.S. law.69
New and Evolving Issues
U.S. trade policy also increasingly is focused on addressing new and evolving issues in
international IPR protection and enforcement. The IPR landscape is changing, both due to the
growing role of emerging markets in the global marketplace and the increased level of
68
For more information on U.S. trade secret law, see CRS Report R41391, The Role of Trade Secrets in Innovation
Policy, by John R. Thomas.
69
Executive Office of the President, Administration Strategy on Mitigating the Theft of U.S. Trade Secrets, February
2013, p. 4.
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international trade taking place in the digital environment. Some of these issues are discussed
below.
Indigenous Innovation. Originally associated with China, “indigenous innovation” is a term that
can reflect multiple policy goals, including promoting innovation from domestic companies rather
than relying on foreign technology, building domestic R&D capabilities, and increasing the share
of overall value added by domestic companies to the domestic economy. Such innovation policies
can surface in areas such as government procurement, technical standards, and technology
transfer.70 For example, indigenous innovation policies may require the transfer of technology as
a condition for allowing access to a market or for a company to continue to do business in the
market.71 While the goal of increasing domestic manufacturing and innovation is understandable,
the U.S. government, industry groups, and other stakeholders express concern that indigenous
innovation policies are discriminatory and may unfairly disadvantage U.S. right holders in those
countries. China’s indigenous innovation policies, for example, have been a source of trade
tension with the United States. Although the Chinese government has pledged to separate
indigenous innovation from government procurement, U.S. business leaders remain concerned
that China’s policies may lead to discrimination against foreign firms or run afoul of WTO
commitments.72 While China’s indigenous innovation policies remain a focal point of U.S. trade
policy, according to the USTR’s 2013 Special 301 Report, such policies appear to be gaining
ground in other countries as well, such as India.
Localization Barriers to Trade. Functioning as a type of non-tariff barrier to market access,
“forced” localization measures generally refer to those designed to protect, favor, or stimulate
domestic industries, service providers, or intellectual property at the expense of foreign
counterparts. Localization barriers can take a number of forms, such as requirements for: service
providers to process data in the foreign country as a condition of market access; businesses to
transfer technology and intellectual property as a condition of approval of foreign investments; or
firms to use local content as a condition for manufacturing or for government procurement. For
example, in November 2011, India issued a “National Manufacturing Policy,” which calls for
greater local content requirements in government procurement in certain sectors, such as
information and communications technology and clean energy. India’s National Manufacturing
Policy is rooted in the country’s goal of developing its manufacturing base and boosting
employment. Based on this policy, in recent years, the Indian government has undertaken or is
considering undertaking a series of regulatory measures mandating the use of local goods and
services in business activity in India, across a range of industrial sectors. While some localization
barriers may serve data privacy or security objectives, concerns have arisen that some of these
measures can be economically distorting. According to the USTR, these measures can distort
trade, inhibit FDI, and lead other countries to follow suit.73 Certain localization barriers have been
addressed in previous multilateral trade negotiations. For instance, the WTO Agreement on
Trade-Related Investment Measures (TRIMs) prohibits “local content” requirements imposed in a
discriminatory manner with respect to foreign investment.74 Other localization barriers,
70
The term “indigenous innovation” can be tied to China’s Medium- to Long-term Plan for the Development of
Science and Technology, released in January 26, which calls for China to become an “innovation-oriented society” and
a global leader in science and technology.
71
U.S. International Trade Commission, China: Effects of Intellectual Property Infringement and Indigenous
Innovation Policies on the U.S. Economy, Investigation No. 332-519, USITC Publication 4226, May 2011.
72
For more information, see CRS Report RL33536, China-U.S. Trade Issues, by Wayne M. Morrison.
73
USTR, 2013 National Trade Estimate Report on Foreign Trade Barriers, March 2013.
74
As defined by USTR, “local content” requirements are requirements to purchase domestically-manufactured goods
(continued...)
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particularly with respect to the digital environment, are considered to be newer trade issues, and
are a focus of the TPP and TTIP negotiations.
Patent Revocation, Denial and Changes in Thresholds of Patentability. U.S. policymakers,
business leaders, and other are increasingly concerned about policy and legal developments in
various countries that, from their perspective, are leading to a deterioration of patent protections.
Key issues have been raised about provisions in India’s Patent Law that prohibit patents on
certain chemical forms absent a showing of increased efficacy. According to the USTR, this
practice could limit the patentability of potentially beneficial innovations (see text box).
Recent Pharmaceutical Patent Decisions in India
Since 2012, India has denied or revoked patents for several cancer and hepatitis C drugs developed by several
Western pharmaceutical companies, including Bayer, GSK, Novartis, Pfizer, and Roche. India’s Supreme Court has
decided to prohibit patents for certain chemical forms absent a showing of “enhanced efficacy,” although the products
are protected by patents in many other countries. India’s patent laws are designed to protect against “ever-greening,”
a practice by which an innovator pharmaceutical company seeks a patent on a modified version of the originally
patented drug to extend the life of the patent, unless there is a showing of enhanced efficacy. Some argue that
through ever-greening, pharmaceutical companies make minor modifications to their patents solely to extend their
monopoly on the patent, thus, delaying the entry of lower-cost generic versions of the drugs onto the market. Others
argue that the modifications can provide new benefits, such as “fewer side effects, decreased toxicity, and better
delivery systems.”75 India also has issued, or threatened to issue, compulsory licenses for pharmaceuticals. For
example, in March 2012, the Indian government issued a compulsory license to an Indian pharmaceutical company to
produce a generic version of Nexavar, a kidney cancer drug produced by Bayer. India defended its decision on the
basis that the price for the patented drug was too high for most Indians. In other developments, the Indian
government “hinted” it would revoke the patent on Herceptin, a breast cancer drug developed by Roche. In August
2013, Roche withdrew the patent for the drug in India.76
Another country of concern is Canada. The USTR noted concerns about Canadian courts’ recent
decisions regarding the heightened “utility” requirement for pharmaceutical patents. U.S.
pharmaceutical companies argue that such decisions contribute to an uncertain business
environment in Canada. For example, one U.S. pharmaceutical company challenged Canada
under NAFTA’s Chapter 11 investor-state dispute settlement mechanism, based on a Canadian
court’s decision to invalidate the company’s patent (see text box).
(...continued)
or domestically-supplied services.
75
USTR, 2013 Special 301 Report.
76
Amy Kazmin, “India Revokes GSK Patent for Version of Cancer Drug,” Financial Times, August 2, 2013; Amy
Kazmin, “India: Patents and Precedents,” Financial Times, May 15, 2013.
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The Eli Lilly-Canada Chapter 11 Case
USTR has criticized the interpretation of utility in judicial invalidation of pharmaceutical patents, which has led to a
NAFTA Chapter 11 investor-state dispute settlement case.77 The U.S. pharmaceutical company Eli Lilly has filed a
Notice of Arbitration against the Government of Canada seeking damages in the amount of $500 million in lost sales
stemming from the invalidation of patents for two medicines. In Canada, the patents for 18 drugs have been
invalidated since 2002 through the use of the so-called promise doctrine, with an estimated loss of revenue to brandname pharmaceutical companies of $1.1 billion.78 This common law doctrine, first invoked by the Supreme Court of
Canada in 2002, states that the utility of a patent must be demonstrated or soundly predicted in the patent
application. Lilly claims that this standard is discriminatory, contrary to utility standards in other countries and in
NAFTA itself, and is adverse to Canada’s own interpretation of utility at the time of NAFTA signing.79 This standard,
some argue, makes it easier for generic companies to challenge the usefulness of a patented drug. The Government of
Canada is currently assessing the information provided in the Notice of Arbitration filed by Eli Lilly on September 12,
2013, and vows to vigorously defend itself against the claims. However, some observers have maintained that there is
no uniform standard for utility among countries, and no one standard enshrined in NAFTA.80
U.S. Trade Law
Special 301
•
Section 301 of the Trade Act of 1974 (P.L. 93-618), as amended, is the principal
U.S. statute for identifying foreign trade barriers due to inadequate intellectual
property protection. The 1988 Omnibus Trade and Competitiveness Act (P.L.
100-418) strengthened section 301 by creating “Special 301” provisions, which
require the USTR to conduct an annual review of foreign countries’ intellectual
property policies and practices. By April 30th of each year, the USTR must
identify countries that do not offer “adequate and effective” protection of IPR or
“fair and equitable market access to United States person that rely upon
intellectual property rights.” According to an amendment to the Special 301
provisions by the Uruguay Round Agreements Act (P.L. 103-465), the USTR
can identify a country as denying sufficient intellectual property protection even
if the country is complying with its TRIPS commitments. These findings are
submitted in the USTR’s annual “Special 301” report.
•
The USTR can designate countries in one of several statutorily- or
administratively-created categories:
•
Priority Foreign Country: A statutory category for those designated by the
USTR as having “the most onerous or egregious acts, policies or practices that
deny intellectual property protection and limit market access to U.S. persons or
firms depending on intellectual property rights protection” and the “greatest
adverse impact (actual or potential) on the relevant United States products.”
77
Under NAFTA, patents shall be granted “provided that such inventions are new, result from an inventive step, and
are capable of industrial application.” NAFTA provides that “inventive step,” and “capable of industrial application,”
are synonymous with “non-obvious,” and “useful,” which underpins the concept of utility. Article 1709(1).
78
“Canada’s Internationally Inconsistent “Promise Doctrine” for Patents,” Eli Lilly background document.
79
“Canada: Eli Lilly Files Notice of Arbitration in $500 million NAFTA Dispute Against Canada,” Bereskin and Parr,
LLP, September 24, 2013.
80
“The ‘Promise of the Patent’ in Canadian Patent Law,” Heenan Blaikie, LLP, Flash Bulletin, December 2013.
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These countries may be investigated under section 301 provisions of the Trade
Act of 1974. The USTR cannot identify countries as Priority Foreign Countries if
they have entered into good faith negotiations or have made significant progress
in improving their intellectual property protection record.81 If a country is named
as a “Priority Foreign Country,” the USTR must launch an investigation into that
country’s IPR practices. The USTR may suspend trade concessions and impose
import restrictions or duties, or enter into a binding agreement with the priority
country that would eliminate the act, policy, or practice that is the subject of the
action to be taken. Since the WTO and its recourse to dispute settlement, the use
of the first option may lead to the initiation of dispute settlement proceedings at
the WTO for member countries, rather than unilateral retaliation. For the limited
number of countries outside the WTO, trade sanctions remain a possibility.
•
Priority Watch List: An administrative category created by the USTR for those
countries whose acts, policies, and practices warrant concern, but who do not
meet all of the criteria for identification as Priority Foreign Country. The USTR
may place a country on the Priority Watch List when the country lacks proper
intellectual property protection and has a market of significant U.S. interest.
•
Watch List: An administrative category created by USTR to designate countries
that have intellectual property protection inadequacies that are less severe than
those on the Priority Watch List, but still attract U.S. attention.
•
Section 306 Monitoring. A tool used by USTR to monitor countries for
compliance with bilateral intellectual property agreements used to resolve
investigations under section 301.
•
Out-of-Cycle Review. A tool used by USTR on countries to monitor their
progress on intellectual property issues, and which may result in status changes
for the following year’s Special 301 report.
For the 2013 Special 301 Report, the USTR reviewed the IPR policies and practices of 95
countries, and designated them in one of the categories discussed above (see Table 4).
The Special 301 statute provides the overall guideline for identifying countries for the various
lists. However, placement on one of the lists is country-specific and takes into consideration a
host of factors, including the level and scope of the country’s IPR infringement and their impact
on the U.S. economy, the strength of the country’s IPR laws and enforcement of IPR laws,
progress made by the country in improving IPR protection and enforcement in the past year, and
the sincerity of the country’s commitment to multilateral and bilateral trade agreements. There is
no “weighting criteria” for the factors or a formula to determine the placement of a country on the
watch list. Furthermore, no particular threshold exists for determining when a country should be
upgraded or downgraded on the list. In making determinations, the USTR gathers information
based on its annual trade barriers reports, as well as consultations with a wide variety of sources,
including industry groups, other private sector representative, Congress, and foreign
governments.
81
For the Special 301 provisions, see 19 U.S.C. §2242; Trade Act of 1974, as amended, (P.L. 93-618), §182.
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Table 4. USTR 2013 Special 301 Report: Country Designations
Special 301 Category
2013 Special 301 Designation
Priority Foreign Country
•
Priority Watch List
10 countries: Algeria, Argentina, Chile, China, India, Indonesia, Pakistan, Russia,
Thailand, and Venezuela
Watch List
30 countries: Barbados, Belarus, Bolivia, Brazil, Bulgaria, Canada, Colombia, Costa
Rica, Dominican Republic, Ecuador, Egypt, Finland, Greece, Guatemala, Israel, Italy,
Jamaica, Kuwait, Lebanon, Mexico, Paraguay, Peru, Philippines, Romania, Tajikistan,
Trinidad and Tobago, Turkey, Turkmenistan, Uzbekistan, and Vietnam
Section 306 Monitoring
China and Paraguay
Out-of-Cycle Reviews
•
Spain—focusing on steps to combat copyright piracy over the Internet
•
El Salvador—focusing on implementation of new legislation on
pharmaceuticals and enforcement efforts
•
“notorious markets”—including online markets, that reportedly engage in
piracy and counterfeiting
Ukraine—based on concerns of the country’s continued deterioration in IPR
protection, enforcement, and market access for persons relying on IPR; the
first time in seven years that the USTR has listed a country. In May 2013,
USTR announced that the United States has initiated an investigation under
section 301 of the Trade Act of 1974 of the IPR acts, policies, and practices of
Ukraine. However, in March 2014, the USTR announced that it would not
take any action against Ukraine in light of its political situation.
Source: CRS adaption from USTR, 2013 Special 301 Report; and USTR, “Notice of Determination in Section
301 Investigation of Ukraine,” 79 Federal Register 14326, March 13, 2014.
Notes: For the 2013 Special 301 Report, the USTR reviewed the IPR policies and practices of 95 countries, and
designated them in one of several categories.
Section 337
Section 337 of the Tariff Act of 1930 (19 U.S.C. 1337), as amended, prohibits unfair methods of
competition or other unfair acts in the importation of products into the United States. It also
prohibits the importation of articles that infringe valid U.S. patents, copyrights, processes,
trademarks, semiconductor products produced by infringing a protected mask work (e.g.,
integrated circuit designs), or protected design rights. While the statute has been utilized to
counter imports of products judged to be produced by unfair competition, monopolistic, or anticompetitive practices, it has become increasingly used for its IPR enforcement functions in recent
years. Under the statute, the import or sale of an infringing product is illegal only if a U.S.
industry is producing an article covered by the relevant IPR or is in the process of being
established. However, unlike other trade remedies such as antidumping or countervailing duty
actions, no showing of injury due to the import is required.
The U.S. International Trade Commission (ITC) administers section 337 proceedings. USITC
must investigate complaints either brought to it or ones commenced under its own initiative. An
administrative law judge provides an initial determination to the ITC which can accept the initial
determination or order a further review of it in whole or in part. If the ITC finds a violation, it
may issue two types of remedies: exclusion orders or cease and desist orders. The ITC may issue
either a limited or general exclusion order enforced by U.S. Customs and Border Protection
(CBP). A general exclusion order directs CBP to keep out all infringing articles regardless of the
source. More commonly, a limited exclusion order is employed to exclude infringing articles
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from the firm subject to the ITC’s investigation. Alternatively, the ITC may enforce a cease and
desist order to stop the sale of the infringing product in the United States. However, the ITC may
consider several public interest criteria and decline to issue a remedy. Also, the President may
disapprove a remedial order during a 60 day review period for “policy reasons.” A presidential
review of a remedial order often considers several relevant factors, including “(1) public health
and welfare; (2) competitive conditions in the U.S. economy; (3) production of competitive
articles in the United States; (4) U.S. consumers; and (5) U.S. foreign relations, economic and
political.”82
The number of Section 337 cases managed by the ITC has trended upward in recent years. The
overwhelming majority of Section 337 cases are patent-focused, involving high-technology
products, such as telecommunication and computer equipment (e.g., smartphones and tablets);
integrated circuits (e.g., memory chips); and display devices (e.g., digital televisions). Other
investigations concerned consumer items, and chemical and medical technologies. In addition, in
FY2012, the ITC saw an increase in the number of investigations involving alleged
misappropriation of trade secrets related to imported goods.83
In the 112th Congress, legislative efforts related to Section 337 focused on addressing
jurisdictional problems associated with holding foreign websites accountable for piracy and
counterfeiting. Multiple bills were introduced, renewing congressional and public debate about
the balance between protecting U.S. intellectual property and promoting innovation. Congress
could take these issues up again, as well as other issues, including CBP’s enforcement of Section
337 exclusion orders.
Generalized System of Preferences
The Generalized System of Preferences (GSP) is a program that provides preferential duty-free
entry to certain products from designated developing countries. The purpose of the program is to
foster economic growth in developing countries by increasing their export markets. The Trade Act
of 1974 authorized the GSP for a ten-year time frame, and the program has been renewed from
time to time. The GSP program expired in 2013, and legislation considering its renewal could be
considered by Congress.84
Although the GSP is non-reciprocal, it can be used to promote stronger intellectual property
protection and enforcement abroad. Under the GSP statute, the President must consider a set of
mandatory criteria that a country must fulfill in order to be designated as a GSP beneficiary.
Additionally, the President may evaluate a country on the basis of certain discretionary criteria,
including the country’s provision of IPR protection.85
The GSP program undergoes an annual review by the GSP Subcommittee of the Trade Policy
Staff Committee (TPSC), which is headed by the USTR. As part of its evaluation, the TPSC
addresses concerns about specific country practices (such as intellectual property protection) and
82
S. Rep. No. 93-1298, 93d Cong. 2d Sess. 199 (1974).
ITC, FY2014 Congressional Budget Justification.
84
See CRS Report RL33663, Generalized System of Preferences: Background and Renewal Debate, by Vivian C.
Jones.
85
91 U.S.C. §2462(b)(2).
83
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makes recommendations to the President. Following the 2012 GSP Annual Review, the USTR has
decided to continue to review IPR practices in Indonesia, Russia, Ukraine, and Uzbekistan, on the
basis of IIPA petitions for ongoing GSP reviews.86
Issues for Congress
Congress has legislative, oversight, and appropriations responsibilities related to IPR and trade
policy. What follows are certain key issues that Congress could consider as it fulfills those
responsibilities.
U.S. Efforts to Promote IPR Through Trade Policy
Since the inclusion of IPR provisions in NAFTA and the TRIPS Agreement, IPR protection and
enforcement have been major U.S. trade policy negotiating objectives. Alongside the growing
role of IPR in trade policy, there has been an ongoing debate regarding the appropriateness of this
role. From one perspective, IPR could promote trade through innovation, economic growth, and
technology transfer from advanced to developing countries. From another perspective, IPR,
which grant legal temporary monopolies to rights holders for their creations, could be considered
barriers to trade with no place in trade liberalization negotiations. Given the continued use of
trade policy to advance IPR objectives, debates also have focused on the appropriate balance
between the protection and enforcement of IPR and other public policy objectives, such as access
to medicines and the free flow of information, as well as the extent to which these goals are
complementary or conflicting. Additionally, there have been debates about the trade policy
channels used by the United States to promote IPR goals. Some question the appropriateness of
using regional and bilateral FTAs for pursuing stronger IPR, contending that such actions take
away from the effectiveness of multilateral IPR promotion efforts. Others argue that strong IPR
commitments in U.S. regional and bilateral FTAs can provide momentum for developing such
disciplines at the multilateral level.
U.S. IPR negotiating objectives may be affected by the language of any future TPA. In
discussions about renewal of TPA, Congress may choose to consider possible reiteration or
expansion on its IPR goals related to global health from the 2002 TPA. Congress also may choose
to consider whether or not to follow the template provided by the Peru, Panama, and Colombia
FTAs in future trade negotiations, such as negotiations on the Trans-Pacific Partnership
Agreement. In addition, through the debate over TPA negotiating objectives, Congress is
expressing concerns over new and emerging issues in IPR, such as those related to indigenous
innovation, “forced” localization barriers to trade in the digital environment, and cybercrime.
Addressing IPR Trade Challenges in Emerging Economies
Some policymakers have voiced concern over the effectiveness of the current U.S. trade policy
agenda in addressing IPR trade challenges associated with emerging economies, such as China,
India, and Brazil—countries with which there are no existing U.S. FTAs and with which the
United States is currently not negotiating any FTAs. Congress could examine how existing trade
86
USTR, GSP: 2012 Annual Review, http://www.ustr.gov.
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policy tools are operating with respect to emerging economies. Beyond this, Congress could
explore other options for advancing U.S. IPR trade policy objectives in emerging economies,
including in the following areas:
•
U.S. FTA negotiations. The TPP and TTIP negotiations are intended to help
shape global rules addressing challenges in third countries, such as with respect
to localization barriers to trade—issues relevant to emerging economies.
Moreover, TPP negotiators seek to craft the TPP as an “open” and “living”
agreement that other countries, such as China and India, could ultimately join if
they were willing to take on its high standard commitments. Congress could
consider to what extent the United States can or should encourage these emerging
economies to join the TPP negotiations, and if so, how that might be
accomplished.
•
Bilateral Investment Treaties (BITs). Through the negotiation of BITs, the
United States seeks to reduce barriers to foreign investment and strengthen
protections for foreign investment.87 The U.S. Model BIT, the template the
United States uses to negotiate BITs and investment chapters of FTAs, treats IPR
as a covered form of investment subject to protections. Currently, the United
States is negotiating BITs with both China and India. Congress could examine the
progress of these negotiations, including how IPR issues are being addressed.
Should these BIT negotiations be concluded, they would be subject to Senate
ratification in order to enter into force.
•
U.S. trade promotion and preference programs. Some stakeholders point to
U.S. trade promotion and preference programs as a potential tool for Congress to
encourage policy reform in emerging economies. For example, in light of
heightened concern over India’s intellectual property environment, some
stakeholders have called on Congress to remove India from the Generalized
System of Preferences beneficiary list.88 Should Congress take up GSP
reauthorization, India’s eligibility status could be among the issues examined.
•
WTO TRIPS Agreement. Congress may examine how the WTO TRIPS
Agreement is working with respect to emerging economies, as well as whether
there are additional opportunities for seeking redress for violations of TRIPS
Agreement commitments through the WTO Dispute Settlement Mechanism with
these trading partners. For instance, the United States has seen some success in
challenging China’s copyright practices through the WTO. Some stakeholders
also call for the United States to pursue greater trade enforcement action on IPR
with respect to other countries.
87
See CRS Report R43052, U.S. International Investment Agreements: Issues for Congress, by Shayerah Ilias Akhtar
and Martin A. Weiss. U.S. BITs provide investment protections through provisions such as requirements for nondiscriminatory treatment, protections against expropriation, and the right to neutral, binding arbitration to resolve
disputes investors and host countries.
88
See CRS Report RL33663, Generalized System of Preferences: Background and Renewal Debate, by Vivian C.
Jones; and Stephen Ezell, Withdraw India’s GSP Preference If It Continues to Impose Localization Barriers to Trade
on Foreign Enterprises, ITIF, January 23, 2013, http://www.innovationfiles.org/withdraw-indias-gsp-preference-if-itcontinues-to-impose-localization-barriers-to-trade-on-foreign-enterprises/.
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Effectiveness of the U.S. IPR Organizational Structure
The United States has a complex apparatus for supporting intellectual property rights, with
responsibilities cutting across many different federal government agencies. For an overview of
federal agencies and coordinating bodies involved in U.S. IPR-related efforts, see Appendix C.
Some Members of Congress, private sector representatives, and other stakeholders express
concern about whether the present U.S. IPR organizational structure is doing enough to enforce
foreign countries’ IPR obligations, as well as whether the structure is capable of doing more.
One set of issues centers on coordination. Given the range of federal agencies involved in IPR
protection and enforcement, questions have emerged about whether federal IPR activities are
sufficiently coordinated in the present U.S. IPR organizational structure (see text box). On one
hand, the Administration’s establishment of various interagency bodies related to IPR, such as the
Intellectual Property Enforcement Coordinator (IPEC), National Intellectual Property Rights
Coordination Center (NIPRCC), and Interagency Trade Enforcement Center (ITEC), affirms the
U.S. commitment to enforcing IPR and the importance of interagency coordination. On the other
hand, there are debates about whether the various IPR-related interagency coordinating
mechanisms overlap. From one perspective, these interagency bodies focus on differing aspects
of IPR protection and enforcement, and in doing so, collectively help to advance U.S. IPR goals
in trade policy. From another perspective, the existence of multiple interagency coordinating
bodies can contribute to additional bureaucracy.
2013 Joint Strategic Plan on Intellectual Property Enforcement
The U.S. Intellectual Property Enforcement Coordinator (IPEC), assisted by its Advisory Committee, is charged with
developing a “Joint Strategic Plan” for combating counterfeiting and piracy. Legislation requires the Joint Strategic Plan
to include in its objectives: reducing counterfeiting and infringing goods in the domestic and international supply chain,
identifying and addressing barriers to effective enforcement domestically, ensuring that information is shared among
the relevant departments and agencies, eliminating domestic and international counterfeiting and infringement
networks, strengthening the capacity of foreign countries to protect and enforce IPR, and cooperating with other
countries to establish international standards and policies to enforce IPR. In June 2013, the IPEC released its second
Joint Strategic Plan on Intellectual Property Enforcement, which noted progress and areas for future activity in six
major areas of focus: (1) leading by example; (2) increasing transparency; (3) ensuring efficiency and coordination; (4)
enforcing U.S. rights internationally; (5) securing the supply chain; and (6) building a data-driven government.
Source: Executive Office of the President, 2013 Joint Strategic Plan on Intellectual Property Enforcement, June 2013
http://www.whitehouse.gov/sites/default/files/omb/IPEC/2013-us-ipec-joint-strategic-plan.pdf.
Another set of issues centers on federal resources for IPR protection and enforcement. While
protection and enforcement of IPR is a stated trade policy priority for the United States, it is
difficult to get a sense of the magnitude of federal funding and resources devoted to it. Some U.S.
government agencies do not have a separate budgetary line item for IPR-related activities, and
Congress does not always designate specific funds for IPR activities in its appropriations for
agencies. Additionally, there is limited information on the economic and other impacts of piracy
and counterfeiting on the United States. This may complicate the ability of lawmakers to weigh
the threat of IPR infringement against the federal resources available for IPR and other
government priorities. Furthermore, there could be debates about whether attempts to enhance
interagency coordination, without devoting greater resources to IPR enforcement activities, may
translate into greater U.S. IPR enforcement.
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Looking Forward
U.S. efforts to protect and enforce IPR through U.S. trade policy are likely to continue to be of
interest for Congress. The reliance on IPR as a competitive advantage to drive an innovative U.S.
economy is reflected in U.S. trade policy. Congress may set the course of U.S. trade policy
concerning IPR through the development of negotiating objectives in any future trade promotion
authority. It also may consider the treatment of IPR in ongoing U.S. negotiations of the TransPacific and Trans-Atlantic FTAs. It may weigh the balance between greater intellectual property
rights in free trade agreements and the ability to conclude agreements containing such provisions
with other countries. It may wish to examine how to incorporate the IPR aspects of new issues
such as digital trade in U.S. policy.
Congress may also wish to examine the enforcement of U.S. IPR through existing trade
agreements. Congress may examine the effectiveness of such activities such as Special 301.
Congressional debates may continue in areas such as how IPR protection and enforcement relate
to other public policy goals, such as access to affordable medicines. Congress may also wish to
examine the organizational structure for IPR protection and the priority to place on such
enforcement when allocating budgetary resources.
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Appendix A. Summary of WIPO Treaties
Treaty
Date
Concluded
Provisions
Intellectual Property Protection Treaties
Paris Convention for the Protection of Industrial
Property (Paris Convention)
1883 (entered
into force 1884)
Protects industrial property (includes patents,
marks, industrial designs, utility models, trade
names, and geographic indications)
Berne Convention for the Protection of Literary
and Artistic Works (Berne Convention)
1886 (entered
into force 1886)
Protects literary and artistic works, providing
right to control and receive payments for use
Madrid Agreement for the Repression of False
and Deceptive Indications of Source on Goods
(Madrid Agreement - Indications of Source)
1891
Requires States to seize imported goods with
false/deceptive indications of source or to
prohibit importation of such goods; open to
States party to Paris Convention (1883)
Rome Convention for the Protection of
Performers, Producers of Phonograms and
Broadcasting Organizations (Rome Convention)
1961
Protects rights of performers against certain
acts to which they have not agreed; protects
rights of producers of phonograms, and
broadcasting organizations to
authorize/prohibit certain acts; open to States
party to Berne Convention (1886)
Convention for the Protection of Producers of
Phonograms Against Unauthorized Duplication of
their Phonograms (Phonograms Convention)
1971
Protects producers of phonograms against
unauthorized reproduction of their
phonograms or importation of duplications for
public distribution
Brussels Convention Relating to the Distribution
of Programme-Carrying Signals Transmitted by
Satellite (Brussels Convention)
1974
Protects against the unauthorized distribution
of program-carrying signals transmitted by
satellite
Nairobi Treaty on the Protection of the Olympic
Symbol (Nairobi Treaty)
1981
Protects Olympic symbol against unauthorized
commercial uses
Treaty on the International Registration of
Audiovisual Works (Film Register Treaty)
1989
Establishes International Register for
Audiovisual Works
Treaty on Intellectual Property in Respect to
Integrated Circuits (Washington Treaty)
1989
Protects layout designs which display electrical
components of an integrated circuit
Trademark Law Treaty (TLT)
1994
Streamlines national and regional trademark
registration processes
WIPO Copyright Treaty (WCT)
1996 (entered
into force 2002)
Special agreement under Berne Convention;
grants exclusive rights to owners of copyright
in computer programs and compilations of
data/other material
WIPO Performances and Phonograms Treaty
(WPPT)
1996 (entered
into force 2002)
Grants exclusive rights to performers and
phonogram producers
Patent Law Treaty (PLT)
2000 (entered
into 2005)
Aims to harmonize and streamline national
and regional patent application procedures and
patents
Singapore Treaty on the Law of the Trademarks
2006 (not yet in
force)
Builds on TLT (1994); aims to harmonize
trademark registration procedures; has wider
scope (includes communication technology
developments)
Beijing Treaty on Audiovisual Performances
(Beijing Treaty)
2012 (not yet in
force)
Seeks to strengthen economic rights of film
actors and other performers through
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Treaty
Date
Concluded
Provisions
international standards.
Marrakesh Treaty to Facilitate Access to
Published Works for Persons who are Blind,
Visually Impaired or Otherwise Print Disabled
(Marrakesh Treaty)
2013
Treaty to improve access to copyrighted
works for the visually impaired and people
with print disabilities
Budapest Treaty on the International Recognition
of the Deposit of Microorganisms for the
Purposes of Patent Procedure (Budapest Treaty)
1977 (entered
into force 1980)
Special agreement under Paris Convention
(1883); requires States to recognize the
deposit of a microorganism with any
“international depositary authority”
Madrid Agreement Concerning the International
Registration of Marks (Madrid Agreement Marks)
1891
Requires seizure of imported goods with
false/deceptive indication of source or
prohibition of importation of such goods; open
to States party to Paris Convention (1883)
Hague Agreement Concerning the International
Registration of Industrial Designs (Hague
Agreement)
1925 (entered
into force 1928)
Allows protection of industrial designs in all
member states on basis of single application
with WIPO; three acts currently in force:
1934, 1960, and 1999 Acts
Lisbon Agreement for the Protection of
Appellations of Origin and their International
Registration (Lisbon Agreement)
1958
Provides international protection for
geographical indications
Patent Cooperation Treaty (PCT)
1970 (entered
into force 1978)
Establishes an international patent filing
system; allows a single international patent
application to have legal standing in all
countries signatory to PCT; open to States
party to Paris Convention (1883)
Protocol Relating to the Madrid Agreement
(Madrid Protocol )
1989 (entered
into force 1995)
Relates to Madrid Agreement (1891); seeks to
make Madrid system more amenable to
domestic laws of certain who are not yet
signatories to Madrid Agreement; open to
States party to Paris Convention (1883)
Nice Agreement Concerning the International
Classification of Goods and Services of the
Purposes of the Registration of Marks (Nice
Agreement)
1957 (entered
into force 1961)
Establishes a classification of goods and
services in order to register trademarks and
service marks; open to States party to Paris
Convention (1883)
Locarno Agreement Establishing an International
Classification for Industrial Designs
1968 (entered
into force 1971)
Establishes a classification for industrial
designs; open to States party to Paris
Convention (1883)
Strasbourg Agreement Concerning the Industrial
Patent Classification (Strasbourg Agreement)
1971 (entered
into force 1975)
Establishes the International Patent
Classification (IPC); open to States party to
Paris Convention (1883)
Vienna Agreement Establishing Classification of
the Figurative Elements of Marks (Vienna
Agreement)
1973 (entered
into force 1985)
Establishes a classification for marks which
consist/contain figurative components; open to
States party to Paris Convention (1883)
Global Protection System Treaties
Classification Treaties
Source: WIPO.
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Appendix B. Patent and Copyright Provisions in the
TRIPS Agreement and U.S. FTAs
Intellectual
Property
Forms
TRIPS Provisions
(1994)
General TRIPS-Plus
Provisions in FTAs
Scale-down of TRIPS-Plus
Standards
Mandatory extensions in cases
of unreasonable delays in patent
grants/regulatory approval
Optional extensions in cases
of unreasonable delays in
patent grants/regulatory
approval
Patents
Patent term
extensions
No provisions
Jordan (Article 4.23.a),
Chile (Article 17.9.6; 17.9.2a),
Singapore (Article 16.7.7;
18.8.4a), Australia (Article 17.9.8;
17.10.4), Morocco (Article 15.9.7;
15.10.3), CAFTA-DR (Article
15.9.6; 15.10.2), Bahrain (Article
14.8.6),Oman (Article 15.8.6),
Korea (Article 18.8.6)
Market approval
linked to patent
status
No provisions
NAFTA (no mention),
Jordan (no linkage, but patent
owner must be notified if
another entity is seeking
marketing approval for generic
version of patented product,
Article 4.23.b)
Protection for
undisclosed test
or other data
Members must protect data
from unfair commercial use
(Article 39.3)
Jordan (Article 4.22)
National regulatory authorities
cannot provide marketing
approval for a generic version of
a patented drug without
permission from rights-holder;
also requires notification of
rights-holder if marketing
permitted
Some restrictions in issuance
of compulsory licenses;
circumstances under which
licenses can be issued not
limited (Article 13)
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Peru (Article 16.9.6), Panama
(Article 16.9.6), Colombia
(Article 16.9.6)
Eliminates mandate that
regulatory authorities cannot
approve a generic drug for
marketing if patent for drug
in place
Peru (Article 16.10.4), Panama
(Article 15.10.4), Colombia
(Article 16.10.4)
Chile (Article 17.10.2b), Singapore
(16.8.4c),Australia (Article
17.10.4), Morocco (Article
15.10.4), CAFTA-DR (Article
15.10.2), Bahrain (Article 14.9.4),
Oman (15.9.4), Korea (Article
18.9.5)
Provides for at least five years
of data exclusivity from date of
approval in country for
pharmaceuticals that contain
new chemical products
NAFTA (Article 1711.6), Bahrain
(Article 14.9.1), Oman (Article
15.9(1-2), CAFTA-DR (Article
15.10.1), Singapore (Article
16.8(1-3)), Australia (Article
17.10.1), Morocco (Article
15.10.1), Chile (Article 17.10.1),
Korea (Article 18.9(1-2))
Issuance of
compulsory
licenses
NAFTA (Article 1709.12)
Limits issuance of compulsory
license to specific cases:
Correcting anti-competitive
practices, public noncommercial contexts, national
emergencies, and other
Provides for at least five
years of marketing exclusivity
from date of approval in
country of first filing if new
drug is granted marketing
approval within six months in
country of second filing
Peru (Article 16.10.2), Panama
(Article 15.10.4), Colombia
(Article 16.10.2)
Not discussed
Chile (no mention), Morocco
(no mention), CAFTA-DR (no
mention), Bahrain (no mention),
Oman (no mention)
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Intellectual
Property
Forms
TRIPS Provisions
(1994)
NAFTA (Article 1709.10),
General TRIPS-Plus
Provisions in FTAs
Scale-down of TRIPS-Plus
Standards
extremely urgent situations
Peru (no mention), Panama (no
mention), Colombia (no
mention), (no mention)
Jordan (Article 4.20), Singapore
(Article 16.7.6), Australia (Article
17.9.7)
Parallel
importing of
patented
products
TRIPS will not be used to
discuss IPR exhaustion
(Article 6)
Biodiversity and
traditional
knowledge
Members may exclude plants
and animals from
patentability (microorganisms and non-biological
and micro-biological
processes must be eligible
for patents); must provide
protection of plant varieties
(Article 27.3(b))
Jordan (no mention), Chile (no
mention), CAFTA-DR (no
mention), Bahrain (no
mention), Oman (no mention)
NAFTA (Article 1709.3),
Bahrain (Article 14.8.(1-2)),
Oman (Article 15.8.2, plants
not discussed),
Parallel importation can be
restricted or prohibited
NAFTA (Article 1709.5, 1709.9),
Singapore (Article 16.7.2),
Morocco (Article 15.9.4), Australia
(Article 17.9.4)
Countries shall make patents
available for plants and animals
Morocco (Article 15.9.2, plants
and animals mentioned, plant
varieties are not mentioned)
Not discussed
Peru (no mention), Panama (no
mention), Colombia (no
mention), Korea (no mention)
Members may exclude plants
and animals from
patentability, but shall take
reasonable effort to provide
patent protection for plants
or animals and maintain
protection once offered
Chile (Article 17.9.2, mentions
plants but not animals), CAFTADR (Article 15.9.2), Peru
(Article 16.9.2), Panama (Article
15.9.2), Colombia (Article
16.9.2)
Jordan, (no mention),
Singapore (no mention),
Australia (no mention), Korea
(no mention)
Copyrights
Rightsmanagement
information
Not discussed
Outlaws removal or alternation of information
NAFTA (no mention), Jordan
(no mention)
Chile (Article 17.5.6), Australia (Article 17.4.8), Singapore (Article
16.4.8), Morocco (Article 15.5.9), CAFTA-DR (Article 15.5.8), Bahrain
(Article 14.4.8), Oman (Article 15.4.8), Peru (Article 16.7.5), Panama
(Article 15.5.8), Colombia (Article 16.7.5), Korea (Article 18.4.8)
Term of
protection
No less than 50 years from
authorized publication
(Article 12)
No less than 70 years from death of author or authorized
publication
NAFTA (Article 1705.4), Jordan
(no mention)
Chile (Article 17.5.4), Singapore (Article 16.4.4), Australia (Article
17.4.4), Morocco (Article 15.5.5), CAFTA-DR (Article 15.5.4), Bahrain
(Article 14.4.4), Oman (Article 15.4.4), Peru (Article 16.5.5), Panama
(Article 15.5.4), Colombia (Article 16.5.5), Korea (Article 18.4.4)
Circumvention
of copyrighted
work
Not discussed
Signatories must agree to prohibit circumvention
NAFTA (no mention)
Jordan (Article 4.6), Chile (Article 17.5.5), Singapore (Article 16.4.7),
Australia (Article 17.4.7), Morocco (Article 15.5.8), CAFTA-DR (Article
15.5.7), Bahrain (Article 14.4.7), Oman (Article 15.4.7), Peru (Article
16.7.4), Panama (Article 15.5.7), Colombia (Article 16.7.4), Korea
(Article 18.4.7)
ISP Liability
Not discussed
ISPs are provided with limited liability in certain situations of
copyright infringement on their servers if they comply with
NAFTA (no mention), Jordan
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Intellectual
Property
Forms
TRIPS Provisions
(1994)
(no mention)
General TRIPS-Plus
Provisions in FTAs
Scale-down of TRIPS-Plus
Standards
regulations
Chile (Article 17.11.23), Singapore (Article 16.9.22), Australia (Article
17.11.29), Morocco, CAFTA-DR (Article 15.11.27), Bahrain, Oman
(Article 15.10.29), Peru (Article 16.11.29), Panama (Article 15.11.27),
Colombia (Article 16.11.29), Korea (Article 18.10.30)
Source: CRS Analysis of FTA provisions.
Note: When there is no mention of an issue in an FTA, the TRIPS standard generally holds.
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Appendix C. Overview of IPR-Related U.S.
Government Agencies and Coordinating Bodies
What follows is a discussion of key U.S. government agencies and coordinating bodies involved
in U.S. efforts to protect and enforce IPR.
Office of the United States Trade Representative (USTR)
The USTR is the lead U.S. trade negotiator and negotiates IPR provisions in U.S. trade
agreements, at the multilateral, plurilateral, regional, and bilateral levels. Currently, the USTR is
negotiating the proposed TPP and TTIP agreements.89 It also enforces U.S. rights under existing
trade agreements. Additionally, through its annual Special 301 Report, USTR is charged with
monitoring the adequacy and effectiveness of IPR protection of our trading partners as well as
their compliance with bilateral and multilateral trade agreements, to identify countries not in
compliance with such agreements, and to negotiate with those countries better compliance. The
USTR further administers the GSP program, under which a country’s eligibility for U.S. trade
preferences may be contingent on its IPR protection.
Department of Commerce (Commerce)
Two agencies within the Department of Commerce, the Patent and Trademark Office and the
International Trade Administration, address IPR issues.90
•
The Patent and Trademark Office (PTO) administers the U.S. laws pertaining
to patents and trademarks. It processes patent and trademark applications, and
issues patents and registers trademarks. The PTO develops IPR protection and
enforcement policy and collaborates with other agencies to develop intellectual
property provisions in FTAs and other international agreements. Additionally, the
PTO offers training, technical assistance, and trade capacity building programs to
assist in promoting strong IPR regimes in foreign countries.91 Its IPR Attaché
Program places individuals with technical expertise and experience overseas to
promote strong international IPR protection and enforcement, such as through
helping to influence laws, regulations, and practices in host countries. The PTO
does not have jurisdiction over determining patent and trademark infringements;
such determinations and remedies are made at the U.S. federal district court level
or through the U.S. International Trade Commission’s section 337 proceedings
(discussed above). The PTO is fully funded through fees generated from patent
and trademark applications.
89
See CRS Report R42694, The Trans-Pacific Partnership (TPP) Negotiations and Issues for Congress, coordinated
by Ian F. Fergusson, and CRS Report R43387, Transatlantic Trade and Investment Partnership (TTIP) Negotiations,
by Shayerah Ilias Akhtar and Vivian C. Jones.
90
General information about the Department of Commerce is available at http://www.doc.gov.
91
NIPLECC, Report to the President and Congress on Coordination of Intellectual Property Enforcement and
Protection, January 2008, p. 21.
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•
The International Trade Administration (ITA) administers many of the
international trade programs of the Department of Commerce, include aspects
involving IPR. The ITA monitors foreign countries’ progress in implementing
intellectual property agreements; reviews Generalized System of Preferences
(GSP) petitions submitted by industry and coordinates the Commerce
Department’s response to these petitions; represents the Commerce Department
at the WTO TRIPS Council; meets with trading partners to advance U.S.
intellectual property interests abroad; and works with U.S. businesses and
industry groups to make sure that IPR-related trade concerns are addressed.92
Department of Justice (DOJ)
The DOJ enforces criminal laws that protect IPR in the United States and internationally through
the prosecution of intellectual property cases. Key units of the DOJ that have IPR enforcement
responsibilities are the Criminal Division, U.S. Attorney’s Office, the Civil Division, the Federal
Bureau of Investigation, and the Office of Justice Programs.
•
The Criminal Division prosecutes intellectual property crimes involving
criminal offenses, namely through its Computer Crime and Intellectual Property
Section (CCIPS).
•
Federal prosecutors in the U.S. Attorneys’ Offices pursue computer crime and
intellectual property offenses.
•
The Federal Bureau of Investigation (FBI) has an intellectual property
enforcement program focusing on intellectual property crimes that have the most
bearing on national and economic security, such as trade secret theft, Internet
priority, and counterfeit tracking goods. Its IPR mission is to “disrupt and
dismantle state sponsored groups and international and domestic criminal
organizations that steal, manufacture, distribute and otherwise profit from the
theft of intellectual property.” IPR is a top priority of the cyber division, though
IPR crimes may be investigated in other divisions. Other IPR priorities for
investigations are counterfeit health and safety products and theft of trade secrets.
•
The Civil Division prosecutes civil actions to recover penalties imposed by the
Department of Homeland Security’s Customs and Border Protection (CBP,
discussed below) with respect to importation of counterfeit goods, brings
affirmative cases when U.S. intellectual property rights are infringed, and
defends CBP enforcement of the International Trade Commission’s Section 337
exclusion orders, among other things.
•
The Office of Justice Program awards grants to support intellectual property
enforcement efforts by state and local law enforcement partners.
In addition to enforcement activities, the DOJ also works with Congress to develop laws that
increase protection of IPR and provides training and technical assistance programs on IPR
enforcement through its Criminal Division.
92
NIPLECC, Report to the President and Congress on Coordination of Intellectual Property Enforcement and
Protection, January 2008, p. 21.
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Department of Homeland Security (DHS)
One of the aims of DHS is to ensure the facilitation of legitimate trade, while enforcing U.S. trade
and IPR laws and investigating IPR violations, specifically trademark, counterfeiting, and
copyright piracy. Key parts of DHS that are involved in IPR enforcement include U.S. Customs
and Border Protection, U.S. Immigration and Customs Enforcement, U.S. Secret Service (USSS),
and the National Intellectual Property Rights Coordination Center.
•
Taking the lead in day-to-day IPR enforcement activities at the U.S. border, the
Customs and Border Protection (CBP) is responsible for detecting and seizing
counterfeit and pirated goods entering the United States and determining
penalties for infringement.93 CBP has the authority to determine whether or not
imports infringe federally registered trademarks and copyrights and to detain or
seize such infringing goods. Owners of copyrights and trademarks are able to
record information about their rights in the CBP’s electronic IPR database. As
noted earlier, in contrast to trademarks and copyrights, CBP does not have the
jurisdiction to make determinations about patent infringements. However, it is
able to block imports determined by the ITC to infringe a U.S. patent by a
Section 337 investigation.94
•
Immigration and Customs Enforcement (ICE) is charged with investigating
violations of U.S. law that are connected with U.S. borders. ICE identifies,
investigates, apprehends, and removes international criminal groups and other
criminals. ICE conducts inquiries into the importation and distribution of
counterfeit goods. ICE activities are closely linked with those of CBP. For
instance, when CBP identifies and seizes counterfeit goods, the issue is referred
to ICE for criminal investigation. Likewise, information obtained from ICE that
is relevant to identifying and apprehending counterfeit shipments is provided to
CBP.
•
The U.S. Secret Service (USSS) investigates violations of laws relating to
counterfeiting of obligations and securities of the United States; financial crimes;
and computer-based attacks on U.S. financial, banking, telecommunications, and
other critical infrastructure. As part of such activities, USSS may find links to
IPR violations.
Department of Health and Human Services
The FDA, which is an agency of the Department of Health and Human Services (DHHS), is
responsible for protecting public health by ensuring the safety and effectiveness of medicines,
food, and other products. As part of its activities, the FDA works to protect consumers against
counterfeit medicines. To combat the entry of foreign counterfeit drugs into the U.S. drug supply,
the FDA works in conjunction with the CBP to conduct border inspections of FDA-regulated
products. The FDA also engages in foreign inspections to ensure that foreign manufacturers meet
93
Certain customs-related IPR policy-making resides within the Treasury.
NIPLECC, Report to the President and Congress on Coordination of Intellectual Property Enforcement and
Protection, January 2008, pp. 15-16. Additional information about CBP is available at http://www.cbp.gov.
94
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FDA quality and labeling requirements. Funding for preventing counterfeits from entering the
United States is part of overall FDA import safety efforts.95
Library of Congress
The Copyright Office of the Library of Congress administers U.S. copyright law by registering
claims to copyright and related documents, including “assignments or transfers of rights” and
maintains information on registrations, recordings, compulsory licenses, and other copyrightrelated actions. Additionally, the Copyright Office provides legal and technical expertise on
national and international copyright issues to the U.S. government. The Copyright Office also
works with other federal agencies to provide assistance and advice in negotiations for
international intellectual property agreements, as well as technical assistance to foreign countries
crafting their own copyright laws.96
Department of State
The Department of State represents U.S. views in both bilateral and multilateral arenas. It works
to build international consensus for IPR enforcement. Information from State’s foreign postings
informs the USTR Special 301 review. In particular, the Bureau of International Narcotics
Control and Law Enforcement (INCLE) works to combat intellectual property piracy, while the
Bureau of Economics and Business Affairs supports stronger international IPR standards to
combat global piracy and counterfeiting.97
U.S. Agency for International Development (AID)
AID funds training and technical assistance to improve the compliance with the TRIPS
Agreement and bilateral trade agreements with the United States. Funding for these projects
generally have been undertaken by regional or country missions; there is no separate budgetary
line item for IPR enforcement and training.98
United States International Trade Commission (ITC)
The ITC is a quasi-judicial federal government agency responsible for investigating and
arbitrating complaints of unfair trade practices. The ITC adjudicates allegations of imported
products that infringe U.S. patents, trademarks, and copyrights through its section 337
proceedings (see above). The primary remedy employed by the ITC is to order the CBP to stop
imports from entering the border. Additionally, the ITC may issue “cease and desist” orders
against individuals determined to be IPR violators. Damages for IPR infringement cannot be
95
Conversation with FDA official, November 26, 2007. Additional information is available on the FDA website,
http://www.fda.gov.
96
NIPLECC, Report to the President and Congress on Coordination of Intellectual Property Enforcement and
Protection, January 2008, p. 18. Also see Copyright Office website, http://www.copyright.gov.
97
NIPLECC, Report to the President and Congress on Coordination of Intellectual Property Enforcement and
Protection, January 2008, pp. 17-18. Additional information about the State Department is available at
http://www.state.gov.
98
Trade Capacity Database and general AID information is accessible at http://www.usaid.gov.
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received through ITC court proceedings; right holders seeking damages must file a civil action
with a U.S. federal district court.99
Coordinating and Advisory Bodies
The USTR leads interagency coordination of U.S. trade policy formulation, negotiation, and
implementation. Beyond this general mechanism, the U.S. government also has interagency
intended to specifically coordinate IPR protection and enforcement activities, as well as private
sector advisory bodies that provide input into the formulation of U.S trade policy. Certain key
coordinating and advisory bodies are outlined below.
Office of the U.S. Intellectual Property Enforcement Coordinator (IPEC)
The IPEC, located in the Office of Management and Budget (OMB) of the Executive Office of
the President, provides executive direction and coordination of federal agencies involved in IPR
enforcement. The position of the U.S. Intellectual Property Enforcement Coordinator, subject to
Senate confirmation, was statutorily established in October 2008, through the Prioritizing
Resources and Organization for Intellectual Property Act of 2008 (P.L. 110-403).100 Among its
key responsibilities are to develop and implement a “Joint Strategic Plan on Intellectual Property
Enforcement” for combating counterfeiting and piracy (see text box); provide assistance to the
USTR in conducting trade negotiations relating to IPR enforcement abroad; and chair an
Advisory Committee composed of representatives from the OMB; Departments of Justice,
Commerce, State, Homeland Security, Agriculture; FDA; AID; and the Register of Copyrights.
National Intellectual Property Rights Coordination Center (NIPRCC)
The Department of Homeland Security houses the NIPRCC, a task force for optimizing the roles
and law enforcement of member agencies and enhancing government-industry partnerships to
support IPR enforcement initiatives. NIPRCC is run jointly by ICE and the FBI. According to
USTR, NIPRCC can be distinguished from ITEC because of the former’s focus on the law
enforcement response to IPR theft (primarily coordinating investigation and prosecution of IPR
infringers under U.S. criminal laws) and the latter’s focus on enforcement of U.S. rights under
trade agreements across a range of issues, one of which is IPR.101
Interagency Trade Enforcement Center (ITEC)
The ITEC is an interagency coordinating body established in February 28, 2012, by Executive
Order. Its aim is to strengthen and coordinate enforcement of U.S. rights under international free
99
ITC website, http://www.usitc.gov.
In creating the IPEC, P.L. 110-403 repealed the authorities creating the National Intellectual Property Law
Enforcement Coordination Council (NIPLECC). Established by Congress in 1999, NIPLECC coordinated U.S.
activities to protect and enforce IPR domestically and abroad, drawing together the major federal agencies the help to
enforce IPR. The Copyright Office participated in the Council in an advisory role. The U.S. Coordinator for
International Intellectual Property Enforcement headed NIPLECC’s interagency coordination efforts. NIPLECC,
Report to the President and Congress on Coordination of Intellectual Property Enforcement and Protection, January
2008, pp. 3-4.
101
USTR, “ITEC Frequently Asked Questions.”
100
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trade agreements and of U.S. trade laws.102 The ITEC is housed within the USTR with a
designated director from the USTR; a designated deputy director from the Department of
Commerce; and support from the Departments of State, the Treasury, Justice, Agriculture,
Commerce, and Homeland Security, as well as the Director of National Intelligence. The
Administration has emphasized the need for creating the ITEC in order to better combat unfair
trade practices by countries such as China. According to USTR, the creation of ITEC will double
the resources to bring trade dispute resolution cases at the WTO “more effectively and more
swiftly.”103
Private Sector Advisory Committee System
The USTR manages a private sector advisory committee system for trade policy, intended to
provide information and advisory on U.S. negotiating objectives and bargaining positions before
the United States enters into trade agreements, the operation of existing U.S. trade agreements,
and other U.S. trade policy matters.104 Statutorily established under section 135 of the Trade Act
of 1974 (P.L. 93-618), the private sector advisory system includes 16 Industry Trade Advisory
Committees (ITACs), which are jointly administered by the USTR and Department of Commerce.
ITAC membership draws from industry and labor. The ITACs reflect a range of U.S. economic
sectors and policy issues, and one of the ITACs focuses on IPR.105
Author Contact Information
Shayerah Ilias Akhtar
Ian F. Fergusson
Specialist in International Trade and
Finance
siliasakhtar@crs.loc.gov, 7-9253
Specialist in International Trade and
Finance
ifergusson@crs.loc.gov, 7-4997
102
The White House, Office of the Press Secretary, “Executive Order—Establishment of the Interagency Trade
Enforcement Center,” February 28, 2012.
103
World Trade Online, “Trade Enforcement Unit Will Not Dilute U.S. Standard for Bringing WTO Cases,” March 1,
2012.
104
USTR, “Advisory Committees,” http://www.ustr.gov/about-us/intergovernmental-affairs/advisory-committee.s
105
USTR, “Industry Trade Advisory Committees (ITAC),” http://www.ustr.gov/about-us/advisory-committees/
industry-trade-advisory-committees-itac.
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