Order Code RL34292 Intellectual Property Rights and International Trade December 20, 2007 Shayerah Ilias Analyst in International Trade and Finance Foreign Affairs, Defense, and Trade Division Ian F. Fergusson Specialist in International Trade and Finance Foreign Affairs, Defense, and Trade Division 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 jobs. Responsibility for developing IPR policy, engaging in IPR-related international negotiations, and enforcing IPR laws cuts across several different U.S. Government agencies. The main structures for coordinating interagency efforts are the National Intellectual Property Law Enforcement Coordinating Council (NIPLECC) and the Strategy Targeting Organized Piracy (STOP!). 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) at the World Trade Organization (WTO), trade policy has been used to enforce IPR abroad. The United States and several trading partners recently announced plans to pursue a multilateral anti-counterfeiting agreement that 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, for the Peru, Panama, and Colombia FTAs, the Administration agreed to scale back some IPR requirements 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 preferential duty-free entry to certain products from the country, and can suspend GSP benefits if IPR protection is lacking. IPR protection and enforcement bring up several key issues for Congress. A central issue is the appropriateness of FTAs as a vehicle for promoting IPR. Congress also faces the challenge of balancing the need for IPR protection and enforcement with the goals of the Doha Declaration on Public Health. Additionally, there has been concern about the effectiveness of the current U.S. IPR enforcement structure. In the 110th Congress, legislation was introduced calling for a new structure to coordinate federal IPR enforcement activities and to increase U.S. international IPR enforcement efforts. This report will be updated as warranted by events. Contents Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 Intellectual Property Rights Basics . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 Types of Intellectual Property . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 Patents . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 Trade Secrets . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 Copyright . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 Trademarks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 Infringement of Intellectual Property . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 Piracy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 Counterfeiting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 Global Intellectual Property Holdings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 Contribution of Intellectual Property to U.S. Economy . . . . . . . . . . . . . . . . . . . . . 6 Prevalence and Economic Consequences of IPR Infringement . . . . . . . . . . 7 Seizures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 Sectoral Infringement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 Motion Picture Piracy Losses: A Closer Look at the Numbers . . . . . . . . . . 12 The Organization Structure of IPR Protection . . . . . . . . . . . . . . . . . . . . . . . . . . . 14 Multilateral IPR System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14 World Trade Organization (WTO) . . . . . . . . . . . . . . . . . . . . . . . . . . . 14 Declaration on TRIPS Agreement and Public Health . . . . . . . . . . . . . 16 Intellectual Property Protection and Development . . . . . . . . . . . . . . . . . . . 18 World Intellectual Property Organization (WIPO) . . . . . . . . . . . . . . . 18 Free Trade Agreements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24 Trade Promotion Authority . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24 Patents . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25 Biodiversity and Traditional Knowledge . . . . . . . . . . . . . . . . . . . . . . . . . . . 28 Copyright . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28 U.S. Trade Law . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35 Special 301 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35 Special 301 Country Lists . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35 Special 301 Report for 2007 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36 Country Identification Factors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36 Section 337 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37 Generalized System of Preferences . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 38 U.S. Agency Functions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39 Department of Commerce (Commerce) . . . . . . . . . . . . . . . . . . . . . . . . 39 Department of Justice (DOJ) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 40 Department of Homeland Security (DHS) . . . . . . . . . . . . . . . . . . . . . . 41 Food and Drug Administration (FDA) . . . . . . . . . . . . . . . . . . . . . . . . . 41 Copyright Office . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 42 Department of State (State) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 42 United States Trade Representative (USTR) . . . . . . . . . . . . . . . . . . . . 43 United States International Trade Commission (ITC) . . . . . . . . . . . . . 43 National Intellectual Property Law Enforcement Coordinating Council (NIPLECC) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43 Strategy Targeting Organized Piracy (STOP!) . . . . . . . . . . . . . . . . . . 44 Issues for Congress . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45 U.S. Efforts to Promote IPR Through Trade Policy . . . . . . . . . . . . . . . . . . 45 Effectiveness of the U.S. IPR Organizational Structure . . . . . . . . . . . . . . . 46 List of Figures Figure 1. 2006 Border Seizures of Counterfeit and Pirated Goods . . . . . . . . . . . . 9 List of Tables Table 1. 2006 Global Intellectual Property Filings Through PCT . . . . . . . . . . . . . 5 Table 2. Estimated Trade Losses Due to Copyright Piracy . . . . . . . . . . . . . . . . 10 Table 3. 2006 Software Piracy Rates and Losses to U.S. Business Software Companies From Selected Countries . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11 Table 4. Estimated Damages for PhRMA Member Companies From Data Exclusivity and Patent Protection Violations . . . . . . . . . . . . . . . . . . . . . . . 13 Table 5. Summary of WIPO-Administered IPR Treaties . . . . . . . . . . . . . . . . . . 20 Table 6. Patent and Copyright Provisions in the TRIPS Agreement and U.S. FTAs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30 Table 7. FY2007 IPR Protection and Enforcement Budgets for U.S. Government Agencies . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45 Intellectual Property Rights and International Trade Introduction Intellectual property rights (IPR) traditionally have been matters of national concern. Individual nation states have developed IPR regimes reflecting their national 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. There is also concern about the potential health and safety consequences of counterfeit pharmaceutical drugs and other products, as well as the link between terrorist groups and traffic in counterfeit and pirated goods. The role of Congress in addressing IPR and trade-related issues stems from the U.S. Constitution, which provides Congress with the power to regulate international trade. While authority to negotiate trade agreements has been delegated periodically to the President, Congressional action is needed to bring the agreements into force. In promoting IPR through international trade policy, Congress may choose to consider whether or not FTAs are an appropriate vehicle for boosting intellectual property protection and enforcement. Congress may also balance IPR protection and enforcement with other public policy goals such as access to medicine in poor or developing countries. Another issue that is before Congress is the effectiveness of the current U.S. coordinating structure for promoting international IPR support. In the 110th Congress, legislation was introduced calling for the creation of a new entity to coordinate federal government interagency intellectual property activities. Legislation also was proposed calling for greater U.S. international IPR enforcement efforts and increased prioritization of resources devoted to such activities. This report discusses the different kinds of IPR; 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; U.S. government agencies involved with IPR and trade; and issues for Congress regarding IPR and international trade. This report will be updated as events warrant. CRS-2 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 Intellectual Property 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’s (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 utility patents). Patents may also 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 patentholder recoups his up-front costs through a temporary monopoly over sale of the invention. In return for this economic rent, the patentholder 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, 1 Uniform Trade Secret Act, §1(4). CRS-3 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 do with 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 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 CRS-4 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 Intellectual Property 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 one of the acts requiring the copyright owner’s permission without his consent, including reproducing, performing, making sound or visual recordings of, and broadcasting the copyrighted work. 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.3 The purpose of counterfeit goods is to deceive consumers about their origin and nature. Counterfeiting and copying of original goods is a major challenge for trademarked products. The counterfeited product can be sold for a premium because of its association of 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 wellknown trademark in order to benefit from the reputation of the product with which he is competing. 2 For information on geographical indications and international trade negotiations, see CRS Report RS21569, Geographic Indications and WTO Negotiations, by Charles E. Hanrahan. 3 Counterfeit goods should be distinguished from generic goods, i.e. in the case of generic forms of pharmaceutical medicines. CRS-5 Global Intellectual Property Holdings Intellectual property holdings that are protected by international agreements are concentrated in firms headquartered in the United States and other developed economies. Developing countries tend to be net importers of intellectual property. For example, half of the approximately 5.6 million patents in force in 2005 were owned by U.S. or Japanese companies. Through the Patent Cooperation Treaty (PCT), an international patent filing system administered by the World Intellectual Property Organization (WIPO), the United States and Japan represented a little over half of all international patent filings in 2006 (see Table 1). In comparison, although developing countries account for 106 of the 136 countries who are signatories to the PCT, they represented only 8% of all international patent filings in the same year.4 However, patent filings are not uniform among developing countries. The industrializing developing economies of Korea, China, India, Singapore, South Africa, Brazil, and Mexico represented over 96% of all patent filings from developing countries in 2006. These countries largely contributed to the dramatic increase (28%) in patent filings from developing countries in 2006, with Korea and China particularly fueling this increase in patent filings.5 Table 1. 2006 Global Intellectual Property Filings Through PCT Country Estimated number of filings Percent of total filings United States 49,555 34.1 Japan 26,906 18.5 Germany 16,929 11.7 Republic of Korea 5,935 4.1 France 5,902 4.1 United Kingdom 5,045 3.5 Netherlands 4,393 3.0 China 3,910 2.7 Switzerland 3,403 2.3 Sweden 3,123 2.1 20,199 13.9 145,300 100.0 All other countries Total Source: WIPO 4 WIPO, “Record Year for International Patent Filings with Significant Growth from Northeast Asia,” February 8, 2007. Statistics on patent applications filed and patents granted by country office are available on the WIPO website, [http://www.wipo.org]. 5 Ibid. CRS-6 Contribution of Intellectual Property to U.S. Economy Intellectual property is an important source of comparative advantage for the United States. Numerous industries in the United States rely on intellectual property for their businesses. Among the industries that are dependant on patent protection are the aerospace, automotive, computer, consumer electronics, pharmaceutical, and semiconductor industries. Copyright-based industries include the software, data processing, motion pictures, 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 According to a 2004 study, U.S. industries that rely on intellectual property accounted for close to 40% of total growth achieved by the U.S. private sector in 2003. These industries comprised about 20% of the private sector’s contribution to the U.S. gross domestic product (GDP) that same year. With almost 18 million workers, the intellectual property industries are one of the largest source of jobs in the United States; employees receive notably higher wages than individuals in other sectors.7 More broadly, IPR-intensive industries also contribute positively to the U.S. economy through productivity gains and other spillover effects. 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.8 In 2006, U.S. receipts from cross-border trade in royalties and license fees (relating to patent, trademark, copyright, and other intangible rights) amounted to $63.4 billion and payments totaled $26.4 billion. This resulted in a surplus of $37.0 billion, a 6% percent increase from the previous of year.9 Industry-specific figures also demonstrate the importance of the intellectual property to the U.S. economy. For example, the business and entertainment software, motion pictures, recording, and publishing industries, which rely on copyright protection, was estimated to constitute about $819 billion or about 7% of U.S. GDP in 2005. These industries accounted for nearly 13% of U.S. economic growth and 6 Stephen E. Siwek, “Engines of Growth: Economic Contributions of the US Intellectual Property Industries,” commissioned by NBC Universal, 2005, p. 2. 7 Ibid, p. 3. 8 Amanda Horan, Christopher Johnson, and Heather Sykes, “Foreign Infringement of Intellectual Property Rights: Implications for Selected U.S. Industries,” Office of Industries Working Paper, U.S. International Trade Commission, October 2005, p. 4. 9 Jennifer Koncz, Michael Mann, and Erin Nephew, “U.S. International Services,” Survey of Current Business, U.S. Bureau of Economic Analysis (BEA), October 2007, pp. 53-54. This measure of cross-border trade in royalties and license fees by U.S. companies include transactions with both affiliated and unaffiliated foreign companies. CRS-7 4% of U.S. employment (5.4 million workers) in 2005. Foreign sales and exports from these industries amounted to $110.8 billion in 2005.10 The pharmaceutical industry, which is dependent on patents, provides another illustration of intellectual property contributions to the U.S. economy. Domestic sales by research-based pharmaceutical companies that are members of Pharmaceutical Researchers and Manufacturers of America (PhRMA) were $174.7 billion in 2006, a 5% increase from the previous year, while sales abroad increased by 2% to $71.1 billion for 2006.11 The U.S. pharmaceutical industry maintains a strong global position, accounting for over 30% of value added in the global pharmaceutical market place.12 Prevalence and Economic Consequences of IPR Infringement 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. For instance, based on a survey of ten pharmaceutical companies, the Tufts Center for the Study of Drug Development estimated that the cost for developing a new drug cost was over $800 million on average.13 According to PhRMA, it takes about 10 to 15 years of research and development to create a new drug. Pharmaceutical companies collectively spent an estimated $55.2 billion for research and development in 2006.14 In contrast, drug counterfeiters can lower production costs by using inexpensive, and perhaps dangerous or ineffective, ingredient substitutes. The development of technologies and products which can be easily duplicated, such as recorded or digital media, has led to an increase in counterfeiting and piracy. Increasing Internet usage also 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. 10 Stephen E. Siwek, “Copyright Industries in the U.S. Economy: The 2006 Report,” prepared for the International Intellectual Property Alliance (IIPA), November 2006, [http://www.iipa.com], pp. 3-5. 11 PhRMA, “Pharmaceutical Industry Profile 2007,” March 2007, [http://www.phrma.org], p. 47. 12 National Science Foundation (NSF), “Science and Engineering Indicators 2006,” Chapter 6: Industry, Technology, and the Global Marketplace, 2006, [http://www.nsf.gov/statistics/seind06/], pp. 5 and 15. 13 J.A. DiMasi, “Tufts Center for the Study of Drug Development Pegs Cost of a New Prescription Medicine at $802 Million,” press release, November 30, 2001. The study is available at [http://csdd.tufts.edu/]. Some contend that the study overestimates actual research and development costs for creating a new drug; Public Citizen offers a critique, accessible at [http://www.publiccitizen.org]. 14 PhRMA, “Pharmaceutical Industry Profile 2007,” March 2007, [http://www.phrma.org], pp.2 and 6. CRS-8 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, data on seizures of counterfeit and pirated goods can be obtained from customs authorities. One study by the Organization for Economic Cooperation and Development (OECD) indirectly extrapolated available customs data on seizures to conclude that worldwide trade in counterfeit and pirated goods may have amounted to $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 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 undoubtedly would be higher.15 Data on pirated and counterfeit seizures at the U.S. border, provided by the U.S. Department of Homeland Security (DHS) shed light on U.S. trade in IPR infringement problem within the United States. In 2006, the Customs and Border Protection (CBP) and Immigration and Customs Enforcement (ICE) agencies of the DHS made 14,675 seizures, nearly double the 8,022 seizures made in 2005. The domestic value of seizures totaled $155 million in domestic value in 2006, a nearly 70% increase from 2005 ($93 million). Of the 2006 seizures, counterfeit footwear represented $63.4 million (41% of the total). Other popular items included wearing apparel ($23.3 million in value, 16%); handbags, wallets, and backpacks ($14.8 million, 9%); computer and hardware ($14.3 million, 9%); and consumer electronics ($7.1 million, 5%) (see Figure 1). Goods from China accounted for the majority of seizures in 2006 (81%), representing $125.6 million in value. 15 OECD, “The Economic Impact of Counterfeiting and Piracy,”Executive Summary, 2007, p. 4. CRS-9 Figure 1. 2006 Border Seizures of Counterfeit and Pirated Goods Other Goods 19% Pharmaceuticals 1% Footwear 41% Consumer Electronics 5% Computer and Hardware 9% Handbags, Wallets, and Backpacks 9% Clothing Apparel 16% Sources: CBP and L.A. Strategic Trade Center Sectoral Infringement. U.S. industries that rely on IPR protection claim to lose billions of dollars in revenue annually due to piracy and counterfeiting. While the economic consequences of IPR infringement are perceived to be serious, there are no comprehensive estimates of the total losses associated with all types of IPR infringement. Two sectors that have calculated the extent of infringement in their industries and related costs are copyrights and pharmaceuticals. Copyright Industry. The International Intellectual Property Alliance (IIPA), a coalition of seven member associations representing over 1,300 U.S. copyrightbased companies, provides annual estimates of U.S. trade loss associated with copyright infringements in selected countries.16 For 2006, the IIPA claimed that copyright infringements in 61 countries resulted in an estimated $15.3 billion in trade losses for the United States, a 9% decrease from the previous year (see Table 2). 16 The IIPA member associations are: Association of American Publishers (AAP), Business Software Alliance (BSA), Entertainment Software Alliance (ESA), Independent Film and Television Alliance (I.F.T.A.), Motion Picture Association of America (MPAA), and Recording Industry Association of America (RIAA). CRS-10 China and Russia were the leading culprits in terms of trade losses due to copyright piracy, each contributing to at least $2 billion in trade losses in 2006.17 Table 2. Estimated Trade Losses Due to Copyright Piracy Copyright Industry (Millions of U.S. dollars) 2005 2006 Business software 8,684.4 10,345.0 Records and music 2,456.3 2,374.4 Motion pictures 2,913.0 Not available Entertainment software 2,652.8 1,951.0 Books 600.5 582.5 Totals 17,307.0 15,252.9 Source: IIPA IIPA predicts that U.S. trade losses due to copyright infringement may be higher than reported because its estimates do not account for Internet piracy, which IIPA contends is an important contributor to copyright piracy.18 There is a possibility that such IPR infringement loss estimates actually may overestimate the extent to which sales of pirated and counterfeit goods displace legitimate sales. 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.19 For consumers in poor developing countries, especially, this assumption may not be tenable. There is not always a direct relationship between IPR infringement rates and the costs to U.S. firms. 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. IPRbased industries. For instance, the United States had the lowest software piracy rate in the world in 2006 (21%). However, the United States was also the largest contributor to piracy losses for the U.S. business software industry because of the significant size of the domestic computer software market. Losses to the software industry from U.S.-based piracy totaled $7.3 billion in 2006. By contrast, countries 17 IIPA, “IIPA 2007 ‘Special 301’ Report,” Appendix A: Estimated Trade Losses Due to Piracy and Piracy Levels (2005-2006) for IIPA’s 2007 Special 301 Recommendations, February 12, 2007, [http://www.iipa.com], p. 2. 18 “The Copyright Industries in the International Intellectual Property Alliance (IIPA) Submit to USTR their 2007 Report on Piracy in 60 Countries/Territories,” press release, February 12, 2007, [http://www.iipa.com]. 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. CRS-11 with higher software piracy rates, nevertheless, had lower infringement costs to U.S. software firms (see Table 3). The smaller sizes of the markets in these countries contributed to lower piracy-related absolute losses stemming from these countries. The worldwide software piracy rate was 35%, with global piracy amounting to $39.6 billion in losses for the U.S. business software industry.20 Table 3. 2006 Software Piracy Rates and Losses to U.S. Business Software Companies From Selected Countries Country Piracy Rate Piracy Loss (millions of U.S. dollars) Zimbabwe 91% $2 Vietnam 88% $96 Pakistan 86% $143 China 82% $5,429 Russia 80% $2,197 Canada 34% $784 Denmark 25% $183 United States 21% $7,289 Source: BSA. 20 BSA, “Fourth Annual BSA and IDC Global Software Piracy Study,” May 2006, [http://www.bsa.org/globalstudy/], pp. 10-11. CRS-12 Motion Picture Piracy Losses: A Closer Look at the Numbers Recent studies have focused on the economic damages sustained by specific copyright industries. A study conducted by LEK Consulting for the MPAA asserted that the direct economic losses to major U.S. movie companies due to motion picture piracy was approximately $6.1 billion in 2005.a Conversely, this figure can be viewed as an estimate of the future gains that the could be obtained if piracy was reduced substantially. The study found that 80% of U.S. motion picture studio losses resulted from piracy overseas, while 20% resulted from piracy in the United States. China had the greatest motion picture piracy rate, with an estimated 90% of the motion picture market considered to be illegitimate. U.S. film companies lost an estimated $244 million in revenue from piracy in China. At 80%, Russia and Thailand had the second highest motion picture piracy rates, with losses totaling $266 million and $149 million respectively. In terms of dollars losses, however, the leading sources of potential dollar losses for U.S. businesses were Mexico ($483 million), the United Kingdom ($406 million), and France ($322 million), which had significantly lower rates of piracy than the former countries.b A subsequent study found that in addition to the direct losses faced by the motion picture industry, there are also losses sustained by “downstream” industries, such as motion picture theatrical exhibitors or the home-video industry. Accounting for these losses, the motion picture industry experiences $20.5 billion annually in lost output. Using economic multipliers, the study estimated that 141,030 jobs would have been created in the United States annually if motion picture piracy did not occur. This translates into $2.7 billion in lost earnings each year by U.S. workers. The federal, state, and local governments would lose at least $422 million in tax revenues annually from lost personal income, corporate income, and production taxes. This analysis is based on a Regional Input-Output Modeling System (RIMS), which is maintained by the U.S. Bureau of Economic Analysis (BEA).c The study appears to be based on the assumption that the extra revenue that would be obtained absent piracy would be directed toward increased film production. a. “The Cost of Movie Piracy,”analysis prepared by LEK for the MPAA, obtained via electronic request from MPAA, [http://www.mpaa.org], p. 5. b. Ibid., pp. 6-7. c. Stephen E. Siwek, “The True Cost of Motion Picture Piracy to the U.S. Economy,”Institute for Policy Innovation: Policy Report #186, September 2006, [http://www.ipi.org], pp. 4-6, 8-9. Pharmaceutical Industry. The World Health Organization (WHO) estimates that many countries in Africa, Asia, and Latin America have areas where between 10% and 30% of medicines sold are counterfeit.21 The U.S. FDA also estimates that at least 10% of drugs worldwide are counterfeit.22 In the United States and many other developed countries, with relatively strong regulatory systems, the 21 WHO, “Counterfeit Medicines,” fact sheet, revised November 14, 2006, [http://www.who.int/mediacentre/factsheets/fs275/en/index.html]. 22 U.S. FDA, “Counterfeit Drugs Question and Answers,” July 2003, [http://www.fda.gov/oc/initiatives/counterfeit/default.htm]. CRS-13 prevalence of counterfeit drugs is low. According to U.S. customs data, pharmaceuticals accounted for only 1% of all goods seized in 2006, with a domestic value of $2.2 million.23 Still, there is growing concern about the vulnerability of the U.S. medicine supply and distribution chain, especially in light of recent high-profile cases about counterfeit drugs entering the United States. PhRMA provides annual estimates of U.S. pharmaceutical industry losses from foreign violations of data exclusivity and patent protection.24 In its 2007 Special 301 submission to the USTR (covering the period of October 2005 to September 2006), 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 4).25 Damages reported in the 2007 submission were nearly double those reported in the prior year’s submission (covering October 2005 to September 2005). While the total loss associated with IPR infringement grew, damages as a percentage of sales declined from the 2006 submission to the 2007 submission.26 Table 4. Estimated Damages for PhRMA Member Companies From Data Exclusivity and Patent Protection Violations Oct. 2004 - Sept. 2005 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. 23 U.S. CBP and L.A. Strategic Trade Center, “FY2006 Top IPR Commodities Seized,”November 7, 2006, [http://www.cbp.gov]. Because of the costs and resources required to conduct physical inspections, many counterfeit products escape inspection, making it difficult to determine the fraction of pirated goods caught. As a result, seizure statistics from the DHS agencies do not reflect on the overall size of the counterfeit market and total losses. 24 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. 25 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. 26 PhRMA, “Special 301 Submission for 2007,” Appendix: Damage Estimate Methodology, p. v. CRS-14 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 the WTO, 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). The TRIPS Agreement 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 4), 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 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 CRS-15 Understanding (DSU). The binding nature of the DSU, with the possibility of the withdrawal of trade concessions (usually the reimposition of tariffs) for noncompliance, sets this agreement apart from previous IPR treaties that did not have effective dispute settlement mechanisms. In April 2007, the United States filed two WTO dispute settlement cases against China, alleging inadequacies in China’s IPR laws and its barriers to market access for U.S. copyright businesses.27 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.”28 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 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 27 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. 28 Pascal Lamy, “Trade-Related Aspects of Intellectual Property Rights - Ten Years Later,” Journal of World Trade, October 2004, p. 925. CRS-16 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 2016.29 Declaration on TRIPS Agreement and Public Health.30 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, 2001.31 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 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 Decision32 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 2/3 of the member states, of which only 11, including the United States, have ratified to date. Until then, the 2003 29 “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. 30 See also CRS Report RL33750, The WTO, Intellectual Property Rights, and the Access to Medicines Controversy, by Ian F. Fergusson. 31 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]. 32 “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]. CRS-17 waiver continues in force. 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.33 33 “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]. CRS-18 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.a 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.b 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.c 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. a. OECD, “The Impact of Trade-Related Intellectual Property Rights on Trade and Foreign Direct Investment in Developing Countries,” May 28, 2003, [http://www.oecd.org], p. 21. b. Keith E. Maskus, Intellectual Property Rights in the Global Economy, Institute for International Economics, Washington, DC, August 2000. c. Commission on Intellectual Property Rights (CIPR), Integrating Intellectual Property Rights and Development Policy, September 2002. World Intellectual Property Organization (WIPO). In addition to the WTO, the other main multilateral venue for addressing IPR issues is WIPO, a United Nations agency. Established in 1967, WIPO is charged with fostering the effective CRS-19 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 5). 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 1996.34 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 stalled in 2006. 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.35 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.36 34 These WCT and WPPT frequently are referred to as the WIPO Internet Treaties. 35 “Agreement between the World Intellectual Property Organization and the World Trade Organization,”[http://www.wto.org/english/tratop_e/trips_e/wtowip_e.htm]. 36 WIPO, “Intellectual Property Handbook,” [http://www.wipo.org], p. 359. CRS-20 Table 5. Summary of WIPO-Administered IPR Treaties Treaty Date Concluded Provisions Intellectual Property Protection Treaties Paris Convention for the Protection of Industry 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 Protecting 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 CRS-21 Treaty Date Concluded Provisions 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) Global Protection System Treaties CRS-22 Treaty Date Concluded Provisions 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 micoorganism 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 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) 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) CRS-23 Treaty Date Concluded Provisions Classification Treaties 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) Lisbon Agreement for the Protection of Appellations of Origin and their International Registration (Lisbon Agreement) 1958 Provides international protection for geographical indications 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) Source: WIPO. CRS-24 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. 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 were first enacted in trade negotiating 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 North American Free Trade Agreement (NAFTA). FTA negotiations in this century have been conducted under the Trade Promotion Authority Act of 2002 (P.L. 107-210). In the intervening period since the 1988 Act, the TRIPS agreement came into force and the IPR provisions of NAFTA became the template for further bilateral or regional FTAs. Thus the focus of IPR negotiating objectives shifted from creating to strengthening the IPR trade regime. 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 was to negotiate trade agreements in terms of IPR that “reflect a standard of protection similar to that found in U.S. law.”37 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 37 P.L. 107-210, Sec. 2102(b)(4). CRS-25 in TRIPS. Some of the new measures also address technological innovations that have come about since the TRIPS Agreement.38 With the change of control in the 110th Congress, Democrats called for changes in the administration’s trade negotiating strategy in return for support of future trade agreements. In May 2007, the Administration and Congressional leadership concluded a bipartisan agreement on trade policy that addressed Democratic concerns about the implications of enhanced IPR on developing countries’ ability to meet public health needs. 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 (discussed below) 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. What follows is a discussion of some of the central patent and copyright standards sought in FTAs that are currently in force or were modified by the White House and Congress (see Table 6).39 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 scale-down in patent protection in these FTAs may set a precedent for future FTA negotiations.40 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 38 The European Union also plans to pursue what are considered to be TRIPS-plus provisions by some in future Economic Partnership Agreements with African, Caribbean, and Pacific countries. 39 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. 40 Inside US Trade, “Brand-Name Industry Alarmed at IPR Precedent of FTA Template,” May 18, 2007 CRS-26 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 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.41 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.42 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 rightsholder. The TRIPS Agreement permits signatories to issue compulsory licenses for 41 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.” 42 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. CRS-27 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. Parallel Importing. 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 IPRs, 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.43 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. 43 GAO Report 07-1198, “U.S. Trade Policy Guidance on WTO Declaration on Access to Medicines May Need Clarification,” September 2007, p. 19. CRS-28 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 nongovernmental 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 micro-organisms, 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 obligations regarding rightsmanagement information, which is “electronic information that identifies a protected work, its author, and terms and conditions of use,”44 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. 44 CRS Report RL33205, Intellectual Property and the Free Trade Agreements: Innovation Policy Issues, by John R. Thomas, p. 14. CRS-29 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 copyrighted works. These provisions build on the U.S. Digital Millennium Copyright Act (DMCA) of 1998.45 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.46 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. 45 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. 46 For additional information on DMCA provisions, see CRS Report RL32037, “Safe Harbor for Service Providers Under the Digital Millennium Copyright Act,” by Brian T. Yeh and Robin Jeweler. CRS-30 Table 6. 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 Patents Patent term extensions No provisions Mandatory extensions in cases of unreasonable delays in patent grants/regulatory approval Optional extensions in cases of unreasonable delays in patent grants/regulatory approval NAFTA (Article 1709.12) 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) Peru (Article 16.9.6), Panama (Article 16.9.6), Colombia (Article 16.9.6) CRS-31 Market approval linked to patent status National regulatory authorities cannot provide marketing approval for a generic version of a patented drug without permission from rightsholder; also requires notification of rightsholder if marketing permitted Eliminates mandate that regulatory authorities cannot approve a generic drug for marketing if patent for drug in place 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) Peru (Article 16.10.4), Panama (Article 15.10.4), Colombia (Article 16.10.4) 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 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 Jordan (Article 4.22) 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(13)), Australia (Article 17.10.1), Morocco (Article 15.10.1), Chile (Article 17.10.1), Korea (Article 18.9(1-2)) 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 Peru (Article 16.10.2), Panama (Article 15.10.4), Colombia (Article 16.10.2) CRS-32 Issuance of compulsory licenses Some restrictions in issuance of compulsory licenses; circumstances under which licenses can be issued not limited (Article 13) Limits issuance of compulsory license to specific cases: Correcting anti-competitive practices, public non-commercial contexts, national emergencies, and other extremely urgent situations NAFTA (Article 1709.10), Jordan (Article 4.20), Singapore (Article 16.7.6), Australia (Article 17.9.7) 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) Parallel importing of patented products TRIPS will not be used to discuss IPR exhaustion (Article 6) Parallel importation can be restricted or prohibited Not discussed Jordan (no mention), Chile (no mention), CAFTA-DR (no mention), Bahrain (no mention), Oman (no mention) NAFTA (Article 1709.5, 1709.9), Singapore (Article 16.7.2), Morocco (Article 15.9.4), Australia (Article 17.9.4) Peru (no mention), Panama (no mention), Colombia (no mention), Korea (no mention) CRS-33 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)) NAFTA (Article 1709.3), Bahrain (Article 14.8.(1-2)), Oman (Article 15.8.2, plants not discussed), Countries shall make patents available for plants and animals Morocco (Article 15.9.2, plants and animals mentioned, plant varieties are not mentioned) Jordan, (no mention), Singapore (no mention), Australia (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), CAFTA-DR (Article 15.9.2), Peru (Article 16.9.2), Panama (Article 15.9.2), Colombia (Article 16.9.2) COPYRIGHTS Rights-management 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) CRS-34 Term of protection Circumvention of copyrighted work ISP Liability 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) 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) 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. CRS-35 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. 100418) 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. 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.47 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 47 For the Special 301 provisions, see 19 U.S.C. §2242; Trade Act of 1974, as amended, (P.L. 93-618), §182. CRS-36 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 on countries to monitor their progress on intellectual property issues. Out-of-cycle reviews 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. Special 301 Report for 2007 For its 2007 Special 301 Report, the USTR reviewed the IPR policies and practices of 70 countries. The report states that China and Russia are top concerns for the Administration because of their inadequate IPR protection and enforcement. China and Russia, along with ten other countries (Argentina, Chile, Egypt, India, Israel, Lebanon, Thailand, Turkey, Ukraine, and Venezuela), were placed on the Priority Watch List for 2007. The USTR placed another thirty countries on its Watch List. No countries were designated as Priority Foreign Countries. China and Paraguay both continued to be subject to section 306 monitoring. Additionally, the USTR announced out-of-cycle reviews for Russia, Brazil, the Czech Republic, and Pakistan. The Special 301 Report also noted progress made by trading partners. Brazil was downgraded from the Priority Watch List to the Watch List, while the Bahamas, Bulgaria, Croatia, the European Union, and Latvia were removed from the Special 301 listings completely.a a. The USTR Special 301 Report for 2007 is available on the USTR website, [http://www.ustr.gov]. 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 country-specific and, according to a USTR official, take into consideration a host of factors, several of which are mentioned in the Special 301 report.48 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 48 Conversation with USTR official, July 2006. CRS-37 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. 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.49 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.”50 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.51 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 49 Telephone conversation with PhRMA representative, July 2006. 50 Oxfam International, “US bullying on drug patents: one year after Doha,” Oxfam Briefing Paper 33, [http://www.oxfam.org], p. 8. 51 Telephone conversation with USTR official, July 2006. CRS-38 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. During 2006, the ITC reported the initiation of 38 new and ancillary 337 investigations. Of these, 34 concerned patent infringement and 4 were allegations of trademark infringement. The ITC completed a total of 28 investigations and ancillary proceedings under section 337 in 2006, which resulted in 7 exclusion orders and one cease-and-desist order. According to the ITC, Section 337 cases increasingly involve advanced technologies in the computer, telecommunications, automotive, and pharmaceutical sectors. 52 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 tenyear time frame, and the program has been renewed from time to time. Most recently, in 2006, Congress extended GSP through 2008.53 The GSP program currently offers preferential access for close to 5,000 products from 143 countries and territories.54 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.55 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. The 52 “The Year in Trade 2006,” USITC Publication #3927, July 2007, pp. 2-12. 53 For a more thorough discussion of GSP, see CRS Report RL33663, “Generalized System of Preferences: Background and Renewal Debate,” by Vivian C. Jones. 54 55 USTR, “U.S. Generalized System of Preferences Guidebook,” February 2007. 91 USC 2462(b)(2) CRS-39 USTR currently is reviewing a petition by the IIPA to remove Brazil from GSP benefits because of its alleged insufficient IPR protection. In 2006, the USTR concluded a review of Pakistan’s IPR policies and practices in response to a petition also by IIPA for copyright evaluations. The review found that Pakistan has taken steps to reduce IPR optical disc piracy. Consequently, Pakistan remains a GSP beneficiary.56 For 2007, the USTR is scheduled to evaluate IPR protection in Russia, Lebanon, and Uzbekistan on the basis of IIPA petitions for ongoing GSP reviews.57 U.S. Agency Functions 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. 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. Based on a review of agency funding by Congress, it appears that the U.S. government provided at least $1.81 billion for IPR protection and enforcement for FY2007 (see Table 7). The total is likely to be higher since the amount of funding devoted toward IPR activities was not determined for all agencies. 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. Additionally, the National Intellectual Property Law Enforcement Coordinating Council (NIPLECC), an interagency coordinating body, is housed within Commerce.58 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 56 USTR, “USTR Ends Review of Pakistan’s Protection of Intellectual Property Rights.” January 24, 2006. 57 58 USTR, “GSP 2006 Annual Review Lists.” General information about the Department of Commerce is available at [http://www.doc.gov]. CRS-40 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.59 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).60 The PTO is fully funded through fees generated from patent and trademark applications. For FY2007, the Revised Continuing Appropriations Resolution (P.L. 110-5) provided the PTO with budgetary authority to spend $1.8 billion. According to the PTO Congressional Liaison, funding for efforts such as the Strategy Targeting Organized Piracy (STOP), NIPLECC activities, and IPR technical and training programs come from this account. 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.61 Based on the Revised Continuing Appropriations Resolution for 2007 (P.L. 110-5), ITA funding was enacted at $395.6 million, identical to the agency’s 2006 budget. IPR funding is not distinguished in the budget, but an ITA official estimated that FY2007 spending on IPR specifically was $9.6 million.62 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.63 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. 59 NIPLECC, “Report to the President and Congress on Coordination of Intellectual Property Enforcement and Protection,” September 2006, pp. 47-49. 60 Conversation with PTO official, November 26, 2007. 61 NIPLECC, “Report to the President and Congress on Coordination of Intellectual Property Enforcement and Protection,” September 2006, pp. 67-69. 62 63 Conversation with ITA official, October 17, 2007. Department of Justice, “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. CRS-41 The FY2007 SSJC Conference Report (H.Rept. 109-520) provided DOJ with $2.2 million for intellectual property investigations and prosecution. 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.64 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.65 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. 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 (see above).66 H.Rept. 109-476 noted the gravity of the IPR infringement problem and requested CBP to provide information on the resources devoted to preventing IPR infringement for 2004-2007 (projected). 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 obtained from ICE activities that is relevant to identifying and apprehending counterfeit shipments is provided to CBP.67 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. 64 Information about the DHS is available at [http://www.dhs.gov]. 65 Certain customs-related IPR policy-making resides within in the Treasury. 66 NIPLECC, “Report to the President and Congress on Coordination of Intellectual Property Enforcement and Protection,” September 2006, pp. 143-145. Additional information about CBP is available at [http://www.cbp.gov]. 67 Ibid. Also refer to the ICE website, [http://www.ice.gov]. CRS-42 Funding for preventing counterfeits from entering the United States is part of overall FDA import safety efforts.68 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, recordations, compulsory licenses, and other copyright-related 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.69 For FY2007, the Copyright Office was provided $22.7 million (P.L. 110-5). The FY2007 Legislative Branch Appropriations Act (H.R. 5521) provided that not more than $100,000 be available for the International Copyright Institute in the Copyright Office of the Library of Congress to train nationals of developing countries in intellectual property laws and policies. 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 standards to fight global piracy and counterfeiting.70 While the FY2007 SSJC Conference Report (H.Rept. 109-520) did not dedicate any funding for IPR enforcement, it called for embassies in major U.S. markets, such as China, Russia, and Brazil, to develop surveys to measure levels of piracy and counterfeiting and to increase dialogue with officials in Chinese provinces to encourage implementation of China’s IPR obligations. The FY2007 Foreign Operations Conference Report (H.Rept. 109-486) recommended $5 million for programs to fight intellectual property piracy under the INCLE Account. 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. According to the AID Trade Capacity Building (TCB) database, AID projects for TCB for compliance with the 68 Conversation with FDA official, November 26, 2007. Additional information is available on the FDA website, [http://www.fda.gov]. 69 NIPLECC, “Report to the President and Congress on Coordination of Intellectual Property Enforcement and Protection,” September 2006, pp. 97-98. Also see Copyright Office website, [http://www.copyright.gov/]. 70 NIPLECC, “Report to the President and Congress on Coordination of Intellectual Property Enforcement and Protection,” September 2006, pp. 81-84. Additional information about the State Department is available at [http://www.state.gov]. CRS-43 TRIPS Agreement totaled $2.1 million in 2006, down from a peak of $6.9 million in 2003.71 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.72 The FY2007 funding level for USTR was $44.2 million, provided under the Revised Continuing Appropriations Resolution (P.L.110-5). USTR does not differentiate sums for its various negotiating activities, and Congress has not designated specific funds to IPR activities within USTR. 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.73 National Intellectual Property Law Enforcement Coordinating Council (NIPLECC). Created by Congress in 1999, NIPLECC coordinates U.S. activities to protect and enforce IPR domestically and abroad. NIPLECC draws together major federal agencies that help to enforce IPR. Members include USTR Commerce, DHS, DOJ, and State, as well as and their subagencies. The Copyright Office participates in the Council in an advisory role. The U.S. Coordinator for International Intellectual Property Enforcement heads NIPLECC’s interagency coordination efforts.74 In the SSJC Conference Report (H.Rept. 109-520) for FY2007, NIPLECC is provided with $900,000 in dedicated funding under the Department of Commerce heading. 71 Trade Capacity Database [http://www.usaid.gov]. and general AID information accessible at 72 NIPLECC, “Report to the President and Congress on Coordination of Intellectual Property Enforcement and Protection,” September 2006, pp. 91-96. Also see USTR website, [http://www.ustr.gov]. 73 74 United States International Trade Commission website, [http://www.usitcs.gov]. NIPLECC, “Report to the President and Congress on Coordination of Intellectual Property Enforcement and Protection,” September 2006, pp. 12-15 CRS-44 Strategy Targeting Organized Piracy (STOP!). In 2006, NIPLECC adopted the Administration’s STOP! as its plan of action for protecting intellectual property rights abroad. The Administration established STOP! in 2004 to crack down on criminal networks in pirated and counterfeit goods trafficking. This initiative expresses the Administration’s commitment to intellectual property protection and enforcement. STOP! is similar to NIPLECC in that it is a coordinating structure to enhance U.S. IPR protection and enforcement and works with many of the same agencies as NIPLECC, such as Commerce, DOJ, DHS, State, and USTR. The FDA is not a part of NIPLECC, but is a participant in STOP!.75 The budget for STOP! comes from Department of Commerce funding.76 The FY2007 SSJC Conference Report (H.Rept. 109-520) expressed support for the STOP! initiative, but did not specify any funding for initiative. 75 Office of the U.S. IPR Coordinator, “Strategy for Targeting Organized Piracy: Accomplishments and Achievements,” September 2007. 76 GAO-07-710T, Intellectual Property: National Enforcement Strategy Needs Stronger Leadership and More Accountability, p. 6. CRS-45 Table 7. FY2007 IPR Protection and Enforcement Budgets for U.S. Government Agencies Government Agency IPR Dedicated Funding Activities PTO $1.8 billion Administering patent and trademark applications; policy guidance; training and technical assistance NIPLECC $900,000 Interagency IPR enforcement coordination Department of Justice $2.2 million Intellectual property investigations and prosecutions Copyright Office $100,000 International Copyright Institute activities Department of State $5 million Combat intellectual property piracy under International Narcotics Control and Law Enforcement Account USAID $2.1 million (for 2006) Trade capacity building for TRIPS and IPR compliance Total $1.81 billion U.S. government IPR activities Note: While all of PTO’s activities are dedicated toward IPR support, it is difficult to determine exactly how much is directed toward international IPR promotion efforts. Issues for Congress 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 rightsholders 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. The Bush Administration has pursued strengthened international IPR through multilateral, regional, and bilateral venues. However, some question the appropriateness of using regional and bilateral FTAs for this purpose, 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 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 CRS-46 Congress, Congressional Democrats and the Administration agreed to modifications of the patent provisions in the Peru FTA as a result of the May 2007 bipartisan trade agreement. Still, a new Government Accountability Office (GAO) report suggests that USTR should offer clearer policy guidance to align FTA negotiating activities with the WTO Doha Declaration.77 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. At issue for Congress is whether or not to follow the template provided by the Peru, Panama, and Colombia FTAs in future trade negotiations. Without renewal of the TPA, the Administration may be prompted to seek stronger IPR through plurilateral venues. For example, the United States and several key foreign trading partners (Canada, the European Union, Japan, Mexico, New Zealand, South Korea, and Switzerland) recently announced their intention to begin negotiating a new anti-counterfeiting trade agreement. The countries have pledged to go beyond the TRIPS Agreement by promoting international cooperation, developing “best practices” for enforcement, and establishing a strong legal framework for enforcement.78 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. Some members of Congress have criticized the U.S. organizational response to international IPR protection and enforcement, particularly that of the National Intellectual Property Law Enforcement Coordinating Council (NIPLECC). Recent GAO testimony points out some of the problems associated with NIPLECC, including an absence of mission, dearth of activities, and poor image among businesses.79 The FY2007 CJS Committee Report (S. Rept. 109-280) expressed concern about the lack of information on NIPLECC’s progress and evidence of success. 77 GAO-07-1198, U.S. Trade Policy Guidance on WTO Declaration on Access to Medicines May Need Clarification, September 2007. 78 “Peru IPR Text Reflects FTA Template, Shows Reduced PhRMA Sway,” Inside US Trade, July 6, 2007. 79 GAO-07-710T, National Enforcement Strategy Needs Stronger Leadership and More Accountability, April 12, 2007, [http://www.gao.gov/new.items/d07710t.pdf], pp. 8-10. CRS-47 In the first session of the 110th Congress, the “Intellectual Property Rights Enforcement Act” was introduced in the Senate (Bayh, S. 522) and subsequently in the House (Sherman, H.R. 3578) to repeal the mandate for NIPLECC and create a new body called the Intellectual Property Enforcement Network (IPEN) in its place. The bill was referred to the Committees on the Judiciary, Foreign Affairs, and Ways and Means. Under the legislation, IPEN would take on the same role as NIPLECC as a interagency coordinating body. GAO notes that a key difference between IPEN and NIPLECC would be that the head of IPEN would come from the Office of Management and Budget (OMB). The “Prioritizing Resources and Organization for Intellectual Property Act of 2007” (Conyers, H.R. 4279) also was introduced in the first session of the110th Congress. H.R. 4279 calls for the creation of an Office of the U.S. Intellectual Property Enforcement Representative, which, among its various responsibilities, would have the lead in coordinating U.S. government agency IPR enforcement actions and would provide assistance to the USTR in conducting trade negotiations relating to IPR enforcement abroad. Like the “Intellectual Property Rights Enforcement Act,” H.R. 4279 proposes the creation of a new entity to coordinate interagency IPR enforcement efforts. However, it does not specify what the establishment of a new interagency body would imply for the status of NIPLECC. In contrast to NIPLECC, GAO interviews with agency officials suggest that STOP! is viewed positively for its role in enhancing IPR enforcement as a priority among federal agencies, the private sector, and internationally. As a presidential initiative, STOP! does not derive from statutory authority. According to the GAO, STOP! does not fully meet the characteristics associated with being an “effective national strategy.” GAO has expressed concern that STOP! does not discuss risk management or the costs, investments, and processes needed to balance the threats associated with counterfeit products with the resources that are available.80 In testimony before the Senate Banking, Housing, and Urban Affairs Committee, foreign policy observer Moises Naim stated that governments must be selective in setting their priorities, adding, “It is unrealistic to expect governments to combat every aspect of counterfeiting... This approach will further burden already overstretched governments and greatly reduce their effectiveness.”81 One question inferred from the foregoing is whether the United States can or should devote equal resources to prevent the importation of fake Gucci bags and counterfeit medicines. H.R. 4279 would also attempt to prioritize U.S. international IPR enforcement activities. The bill calls for the establishment of ten “intellectual property attachés” in the Department of Commerce to serve in U.S. embassies or other diplomatic missions. Among other responsibilities, the attachés would encourage cooperation with foreign governments in enforcement of IPR laws; assist Americans rightsholders in combating foreign IPR infringement of their products; and facilitate 80 81 Ibid, p. 11. Testimony before the Security and International Trade and Finance Subcommittee of the U.S. Senate Committee on Banking, Housing, and Urban Affairs. “Pirating the American Dream: Intellectual Property Theft’s Impact on America’s Place in the Global Economy and Strategies for Improving Enforcement” by Moises Naim, April 12, 2007. CRS-48 training and technical assistance programs targeted toward improving foreign enforcement of IPR laws. The bill also calls for the deployment of five Intellectual Property Law Enforcement Coordinators under the Department of Justice to serve as liaisons with foreign law enforcement agencies in IPR criminal issues, engage in foreign enforcement capacity-building outreach and training activities, and coordinate U.S. law enforcement activities against IPR-related crimes in the foreign countries. Both the Commerce and Justice missions would be sent to the areas where their efforts would be most effective and beneficial in reducing counterfeiting and piracy. While protection and enforcement of IPR is a stated priority for the United States, it is difficult to get a sense of the magnitude of funding and resources devoted toward IPR support, as there is no one line item in the federal budget for IPR protection. Our analysis suggests that the United States spent at least $1.81 billion to support IPR in FY2007. 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 complicates the ability of lawmakers to weigh the threat of IPR infringement against the federal resources available for IPR and other government priorities.