The Project BioShield Act:
Issues for the 112th Congress
Frank Gottron
Specialist in Science and Technology Policy
February 8, 2012
Congressional Research Service
7-5700
www.crs.gov
R42349
CRS Report for Congress
Pr
epared for Members and Committees of Congress
The Project BioShield Act: Issues for the 112th Congress
Summary
In 2004, Congress passed the Project BioShield Act (P.L. 108-276) to provide the federal
government with new authorities related to the development, procurement, and use of medical
countermeasures against chemical, biological, radiological, and nuclear (CBRN) terrorism agents.
As the expiration of some of these authorities approaches, Congress is considering whether these
authorities have sufficiently contributed to national preparedness to merit extension.
The Project BioShield Act provides three main authorities: (1) guaranteeing a federal market for
new CBRN medical countermeasures, (2) permitting emergency use of countermeasures that are
either unapproved or have not been approved for the intended emergency use, and (3) relaxing
regulatory requirements for some CBRN terrorism-related spending. The Department of Health
and Human Services (HHS) has used each of these authorities. The HHS obligated approximately
$2.5 billion to guarantee a government market for countermeasures against anthrax, botulism,
radiation, and smallpox. The HHS allowed the emergency use of several unapproved products,
including during the 2009 H1N1 influenza pandemic. The HHS used expedited review authorities
to approve contracts and grants related to CBRN countermeasure research and development.
The Department of Homeland Security (DHS) Appropriations Act, 2004 (P.L. 108-90) advance-
appropriated $5.593 billion to acquire CBRN countermeasures through Project BioShield for
FY2004-FY2013. Through FY2012, subsequent Congresses have removed $1.876 billion from
this account through rescissions and transfers, more than one-third of the advance appropriation.
The transfers from this account supported CBRN medical countermeasure advanced
development, pandemic influenza preparedness and response, and basic biomedical research.
Since passing the Project BioShield Act, subsequent Congresses have considered additional
measures to further encourage countermeasure development. The Pandemic and All-Hazards
Preparedness Act (P.L. 109-417) created the Biomedical Advanced Research and Development
Authority (BARDA) in HHS and modified the Project BioShield procurement process. Among
other duties, BARDA oversees all of HHS’s Project BioShield procurements.
The 112th Congress is considering several Project BioShield-related policy questions. One
question is whether the Project BioShield acquisition mechanism has sufficiently improved
national preparedness relative to its costs to merit extension. If so, congressional policymakers
may consider whether changes to the funding levels or how Congress provides Project BioShield
funds would improve the program’s efficiency or performance. Additionally, congressional
policymakers are considering whether the federal government sufficiently plans and coordinates
its CBRN countermeasure efforts from basic research to distribution. Finally, Congress is
considering whether changes to the emergency use authority will improve preparedness and
planning.
Three bills in the 112th Congress address some of these Project BioShield-related issues, H.R.
2356, H.R. 2405, and S. 1855.
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The Project BioShield Act: Issues for the 112th Congress
Contents
Introduction...................................................................................................................................... 1
The Project BioShield Act ............................................................................................................... 2
Market Guarantee ...................................................................................................................... 2
Emergency Use of Unapproved Products.................................................................................. 3
Expedited Procedures ................................................................................................................ 4
Reporting Requirements............................................................................................................ 5
Appropriations, Rescissions, and Transfers..................................................................................... 6
Acquisitions ..................................................................................................................................... 7
BioShield and BARDA.................................................................................................................. 10
Policy Issues and Options for Congress ........................................................................................ 10
Project BioShield Acquisition Authority and Appropriations ................................................. 11
Not Extend Project BioShield ........................................................................................... 11
Extend Project BioShield .................................................................................................. 11
Countermeasure Development and Acquisition Process ......................................................... 13
Emergency Use Authority ....................................................................................................... 14
Current Legislation ........................................................................................................................ 14
H.R. 2405................................................................................................................................. 15
S. 1855..................................................................................................................................... 16
H.R. 2356................................................................................................................................. 17
Tables
Table 1. Project BioShield Rescissions and Transfers ..................................................................... 6
Table 2. Project BioShield Acquisition Activity .............................................................................. 9
Contacts
Author Contact Information........................................................................................................... 17
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The Project BioShield Act: Issues for the 112th Congress
Introduction
Following the terrorist attacks of 2001, both the Administration and Congress determined that the
federal government needed new medical countermeasures (such as diagnostic tests, drugs,
vaccines, and other treatments) to respond to an attack using chemical, biological, radiological, or
nuclear (CBRN) agents. Representatives of the pharmaceutical industry attributed the paucity of
CBRN agent countermeasures to the lack of a significant commercial market.1 They argued that,
because these diseases and conditions occur infrequently, the private sector perceived little
economic incentive to invest the millions of dollars required to bring treatments to market.
In 2004, Congress passed the Project BioShield Act (P.L. 108-276) to encourage the development
of CBRN medical countermeasures. The 108th Congress also appropriated $5.6 billion to acquire
countermeasures through Project BioShield for FY2004 to FY2013. Subsequent Congresses have
evaluated implementation of Project BioShield. In response to perceived problems with Project
BioShield countermeasure procurement, the 109th Congress created the Biomedical Advanced
Research and Development Authority (BARDA) and the position of Assistant Secretary for
Preparedness and Response in the Department of Health and Human Services (HHS) through the
Pandemic and All-Hazards Preparedness Act (PAHPA, P.L. 109-417).
The 112th Congress is considering several Project BioShield-related policy questions. One
question is whether the Project BioShield acquisition mechanism has sufficiently improved
national preparedness relative to its costs to merit extension. If so, congressional policymakers
may consider whether changes to the funding levels or how Congress provides Project BioShield
funds would improve the program’s efficiency or performance. Additionally, congressional
policymakers are considering whether the federal government sufficiently plans and coordinates
its CBRN countermeasure efforts from basic research to distribution. Finally, Congress is
considering whether changes to the emergency use authority will improve preparedness and
planning.
The Pandemic and All-Hazards Preparedness Reauthorization Act of 2011 (H.R. 2405, passed the
House on December 6, 2011), the Pandemic and All-Hazards Preparedness Act Reauthorization
of 2011 (S. 1855, ordered reported by the Senate Committee on Health, Education, Labor, and
Pensions on December 16, 2011), and the WMD Prevention and Preparedness Act of 2011 (H.R.
2356, introduced July 11, 2011) address some of these issues.
This report will provide a brief overview of the authorities established by the Project BioShield
Act of 2004, discuss the availability of Project BioShield appropriations, identify the medical
countermeasures obtained through Project BioShield, review the relationship between Project
BioShield and the Biomedical Advanced Research and Development Authority (BARDA), briefly
review policy issues and options faced by congressional policymakers, and review current
legislation.
1 For example, Alan Pemberton, Pharmaceutical Research and Manufacturers of America, Testimony before the U.S.
House of Representatives Select Committee on Homeland Security, May 15, 2003.
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The Project BioShield Act
President Bush proposed Project BioShield in his 2003 State of the Union address. The 108th
Congress considered this proposal and passed the Project BioShield Act of 2004 (P.L. 108-276,
signed into law July 21, 2004).2 It has three main provisions. The first provision, the one
generally referred to as Project BioShield, creates a government-market guarantee by permitting
the HHS Secretary to obligate funds to purchase countermeasures while they still need several
more years of development. The second main provision establishes a process through which the
HHS Secretary may temporarily allow the emergency use of countermeasures that lack Food and
Drug Administration (FDA) approval. The third main provision provides HHS with expedited
procedures for CBRN terrorism-related spending, including procuring products, hiring experts,
and awarding research grants. This law also requires HHS and the Government Accountability
Office (GAO) to produce certain reports.
Market Guarantee
When companies decide to develop a new product, the potential economic value of the market is
often a key factor. With new CBRN countermeasures, the U.S. government may be the most
economically significant customer. Thus, one difficulty facing potential CBRN developers is
knowing whether the federal government would buy their product and, if so, at what price.
Companies may find it difficult to justify investing millions of dollars developing new
countermeasures without knowing the potential economic value of the government market.
Congress designed the Project BioShield Act to guarantee companies that the government will
buy new, successfully developed CBRN countermeasures for the Strategic National Stockpile
(SNS).3 The act allows the HHS Secretary, with the concurrence of the Homeland Security
Secretary and upon the approval of the President, to promise to buy a product up to eight years
before it is reasonably expected to be delivered.4 Such contracts are only available for products
designed for use against CBRN agents that Department of Homeland Security (DHS) has
determined to pose “a material threat against the Untied States population sufficient to affect
national security.”5
These contracts define the minimum economic value of the market for the company developing
the product. The Project BioShield Act allowed the HHS to pay a company only on the delivery
of a substantial portion of the countermeasure. Such contracts reduce the market risk faced by the
developers, but do not mitigate the risk that the product might fail during testing and be
undeliverable. The Pandemic and All-Hazards Preparedness Act (P.L. 109-417) modified the
Project BioShield Act to allow for milestone-based payments of up to half of the total award
2 For legislative history of this law, see CRS Report RL32549, Project BioShield: Legislative History and Side-by-Side
Comparison of H.R. 2122, S. 15, and S. 1504, by Frank Gottron and Eric A. Fischer.
3 The SNS contains pharmaceuticals, vaccines, medical supplies, and medical equipment to respond to terrorist attacks
and other emergencies.
4 President Bush delegated the presidential approval step to the Director of the Office of Management and Budget
(OMB). The OMB retains this authority in the Obama Administration. See Executive Office of the President,
“Designation and Authorization to Perform Functions under Section 319F-2 of the Public Health Service Act,” 69 Fed.
Reg. 70349, December 3, 2004.
5 42 U.S.C. §247d-6b(c)(2).
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before delivery.6 These contracts reduce the market risk for the company, and the milestone
payments reduce the company’s exposure to development risk.
The Project BioShield Act allows HHS to purchase unapproved and unlicensed countermeasures.
It requires the HHS Secretary to determine that “sufficient and satisfactory clinical experience or
research data ... support a reasonable conclusion that the product will qualify for [FDA] approval
or licensing ... within eight years.”7 Because most drugs that begin the approval process fail to
become approved treatments, critics of this provision suggest that the government will end up
purchasing countermeasures that may never be approved. Some of the countermeasures procured
through Project BioShield since 2004 lack FDA approval. To reduce the government’s financial
risk associated with this provision, the act, as amended, allows HHS to write contracts in which
unapproved products may be purchased at lower cost than approved products. Additionally, HHS
has included provisions for milestone payments and for payments contingent on FDA approval in
Project BioShield contracts. For an overview of those countermeasures obtained through these
authorities, see “Acquisitions” below.
Emergency Use of Unapproved Products
The FDA designed its standard approval and licensing processes to protect people from
ineffective or dangerous treatments.8 During a military, domestic, or public health emergency, the
Project BioShield Act allows the HHS Secretary to temporarily allow the use of medical products
that FDA has not approved or licensed.9 These allowances are known as emergency use
authorizations (EUAs). To exercise this authority, the HHS Secretary must conclude that:
• the agent for which the countermeasure is designed can cause serious or life-
threatening disease;
• the product may reasonably be believed to be effective in detecting, diagnosing,
treating, or preventing the disease;
• the known and potential benefits of the product outweigh its known and potential
risks;
• no adequate alternative to the product is approved and available; and
• any other criteria prescribed in regulation are met.10
Such EUAs remain in effect for one year unless the Secretary terminates them earlier. The
Secretary may renew expiring authorizations.
6 For more on this law, see CRS Report RL33589, The Pandemic and All-Hazards Preparedness Act (P.L. 109-417):
Provisions and Changes to Preexisting Law, by Sarah A. Lister and Frank Gottron.
7 42 U.S.C. §247d-6b(c).
8 For overviews of these processes, see CRS Report R41983, How FDA Approves Drugs and Regulates Their Safety
and Effectiveness, by Susan Thaul, and CRS Report RL34045, FDA Regulation of Follow-On Biologics, by Judith A.
Johnson.
9 The HHS Secretary may also permit the emergency use of a product approved by FDA for a specific use to be used
for purposes for which it is not approved. For example, see footnote 13.
10 21 U.S.C. §360bbb-3(c). For more information on how the Secretary determines whether a product meets these
conditions, see U.S. Department of Heath and Human Services, Food and Drug Administration, Guidance—Emergency
Use Authorization of Medical Products, July 2007, at http://www.fda.gov/RegulatoryInformation/Guidances/
ucm125127.htm.
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The HHS Secretary has issued several EUAs. The HHS Secretary issued an EUA allowing the
vaccination of Department of Defense (DOD) personnel with a specified type of anthrax
vaccine.11 The HHS Secretary issued EUAs to permit use of certain countermeasures during the
2009 H1N1 “swine” influenza outbreak:12 the antiviral influenza treatments Tamiflu
(oseltamivir), Relenza (zanamivir), and Peramivir;13 N95 respirators; and several diagnostic kits
to help identify cases of this disease.14 Two EUAs remain active. One permits the distribution of
antibiotic kits containing doxycycline hyclate to U.S. Postal Service employees volunteering in
the National Postal Model emergency countermeasure distribution program.15 The other active
EUA permits distributing doxycycline hyclate before an emergency and its mass dispensing
without a prescription during an emergency to prevent inhalational anthrax.16
Expedited Procedures
The Project BioShield Act relaxed and expedited the Federal Acquisition Regulation procedures
HHS must follow when procuring property or services used in performing, administering, or
supporting CBRN countermeasure research and development (R&D). These expedited procedures
decrease both the amount of paperwork required for these expenditures and the potential for
oversight. The act also increases the maximum amount (from $100,000 to $25 million) for
contracts awarded under simplified acquisition procedures, and allows these purchases using
other than full and open competition. According to the Government Accountability Office (GAO),
HHS used the simplified acquisitions procedure authority for five contracts. These contracts, all
executed between 2004 and 2005 using funds from the National Institutes of Health (NIH),
totaled approximately $30 million.17 Through December 2010, HHS had not exercised its
authority to use other than full and open competition.18
The Project BioShield Act authorizes the HHS Secretary to use an expedited peer review award
process for grants, contracts, and cooperative agreements related to CBRN countermeasure R&D,
11 70 Fed. Reg. 5452, February 2, 2005.
12 For additional information, see CRS Report R40554, The 2009 Influenza Pandemic: An Overview, by Sarah A. Lister
and C. Stephen Redhead; U.S. Department of Health and Human Services, Project BioShield Annual Report to
Congress January 2009-December 2009, 2011, pp. 9-13; and http://www.cdc.gov/h1n1flu/eua/.
13 The FDA previously approved Tamiflu and Relenza for treating influenza. The EUA allowed their use for infants
and children younger than had been previously allowed. In contrast, FDA had not approved Peramivir and had
restricted its use to experimental trials. The EUA allowed its use outside experimental trials.
14 75 Fed. Reg. 20441-20480, April 29, 2010.
15 This EUA was renewed through October 2012. See 76 Fed. Reg. 72935, November 28, 2011. President Obama
created the National Postal Model emergency countermeasure distribution program by executive order. Executive
Order 13527, “Establishing Federal Capability for the Timely Provision of Medical Countermeasures Following a
Biological Attack,” 75 Fed. Reg.737, January 6, 2010. For more on this program, see http://www.phe.gov/
Preparedness/planning/postal/Pages/default.aspx.
16 76 Fed. Reg. 47197, August 4, 2011.
17 These contracts are distinct from the contracts using Project BioShield funds described later in this report (see
“Acquisitions”). The HHS used these contracts to purchase treatments for botulism and internal radioactive particle
contamination. See U.S. Government Accountability Office, Project BioShield: HHS Can Improve Agency Internal
Controls for Its New Contracting Authorities, GAO-09-820, July 21, 2009, p. 7.
18 U.S. Government Accountability Office, Project BioShield: HHS Can Improve Agency Internal Controls for Its New
Contracting Authorities, GAO-09-820, July 21, 2009; U.S. Department of Health and Human Services, Project
BioShield Annual Report to Congress August 2007 through December 2008, 2009, p. 8; Project BioShield Annual
Report to Congress January 2009-December 2009, 2011, pp. 5-7; and Project BioShield Annual Report to Congress
January 2010-December 2010, 2011, p. 4.
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if the Secretary deems that a pressing need for an expedited award exists. The act limits this
authority to awards worth $1.5 million or less. This expedited award process replaces the normal
peer review process. Some scientists have expressed concerns that an expedited review process
would reduce research quality.19 The normal peer review process can provide proposals that have
greater scientific merit a higher probability of receiving funding, a factor potentially lost in an
expedited process. According to the National Institute of Allergy and Infectious Diseases
(NIAID), grants that go through the normal peer review process typically take 9 to 17 months to
receive funding.20 Between 2004 and 2008, NIAID awarded 5 contracts and 55 grants using
expedited peer review. NIAID funded these awards between 3 and 9 months after the application
deadline.21 In 2009, NIAID funded 4 grants using expedited peer review between 18 and 20
months after the application deadline.22 In 2010, NIAID funded 3 grants using expedited peer
review between 27 and 30 months after the application deadline. According to HHS, these grants
were not funded earlier “due to budget limitations.”23 The increasing elapsed time between
application deadline and funding suggests to some observers that this mechanism no longer
functions to expedite the award process.
Reporting Requirements
The Project BioShield Act of 2004 requires the HHS Secretary to report annually to Congress on
the use of some of the authorities granted by this law. The annual reports must summarize each
instance that HHS used the expedited procurement and grant procedures and allowed the
emergency use of unapproved products. The annual reports must explain why HHS needed to use
these authorities. The HHS has produced five such reports to date.24
This act also required GAO to assess actions taken under authorities granted by the act, determine
the effectiveness of the act, and recommend additional measures to address deficiencies. In July
2009, GAO published two reports in response to this requirement. The first recommended that
HHS improve some internal controls for the expedited contracting procedures (see “Expedited
Procedures” above).25 The second report described the manner in which HHS had used Project
19 John Miller, “Interview with Richard Ebright,” The Scientist, vol. 17 (7), April 7, 2003, p. 52.
20 See http://www.niaid.nih.gov/researchfunding/grant/strategy/pages/7time.aspx.
21 See U.S. Department of Health and Human Services, Project BioShield Annual Report to Congress July 2004-July
2006, 2007, p. 2; Project BioShield Annual Report to Congress August 2006-July 2007, 2008, p. 32; Project BioShield
Annual Report to Congress August 2007 through December 2008, 2009, p. 9; Project BioShield Annual Report to
Congress January 2009-December 2009, 2011, p. 6; and Project BioShield Annual Report to Congress January 2010-
December 2010, 2011, p. 4.
22 U.S. Department of Health and Human Services, Project BioShield Annual Report to Congress January 2009-
December 2009, 2011, p. 6.
23 U.S. Department of Health and Human Services, Project BioShield Annual Report to Congress January 2010-
December 2010, 2011, p. 4.
24 Available online at https://www.medicalcountermeasures.gov/barda/cbrn/project-bioshield-overview/project-
bioshield-annual-report.aspx.
25 U.S. Government Accountability Office, Project BioShield: HHS Can Improve Agency Internal Controls for Its New
Contracting Authorities, GAO-09-820, July 21, 2009.
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BioShield to support development and procurement of CBRN medical countermeasures.26 This
report contained no recommendations for improving Project BioShield.27
Appropriations, Rescissions, and Transfers
The Project BioShield Act did not appropriate any funds. Instead, it authorized the appropriation
of up to $5.593 billion for procuring countermeasures from FY2004 through FY2013. The
Department of Homeland Security Appropriations Act, 2004 (P.L. 108-90) had previously
appropriated this amount into a special reserve fund and provided explicit time windows during
which the money could be obligated. The Project BioShield Act specified that the funds in this
DHS “Biodefense Countermeasures” account are only for the procurement of CBRN
countermeasures using the Project BioShield authorities and may not be used for other purposes,
such as countermeasure development grants or program administration.
While Congress used the advanced appropriations mechanism to fund the 10-year program, it
retains the power to increase or decrease, through rescission or transfer, the amount in the special
reserve fund. Congress removed $25 million from this account through rescissions enacted in the
Consolidated Appropriations Act, 2004 (P.L. 108-199) and the Consolidated Appropriations Act,
2005 (P.L. 108-447). See Table 1.
Table 1. Project BioShield Rescissions and Transfers
Fiscal
Amount
Year Public Law
Purpose
($ in millions)
2004
P.L. 108-199
Rescission
5
2005 P.L.
108-447
Rescission
20
2009
P.L. 111-8
Transfer for countermeasure advanced development
275
Transfer for pandemic flu preparedness
137
2010
P.L. 111-117
Transfer for countermeasure advanced development
305
Transfer for NIAID basic research
304
2011
P.L. 112-10
Transfer for countermeasure advanced development
415
2012
P.L. 112-74
Transfer for countermeasure advanced development
415a
Rescissions and Transfers Enacted
1,876
Source: CRS analysis of P.L. 108-199, P.L. 108-447, P.L. 111-8, P.L. 111-117, P.L. 112-10, P.L. 112-74, and
H.Rept. 112-331.
Note: Amounts rounded to nearest million.
a. The conference report, H.Rept. 112-331, states “up to $415 million.”
26 U.S. Government Accountability Office, Project BioShield Act: HHS Has Supported Development, Procurement,
and Emergency Use of Medical Countermeasures to Address Health Threats, GAO-09-878R, July 24, 2009.
27 Other Project BioShield-related GAO reports include National Preparedness: Improvements Needed for Acquiring
Medical Countermeasures to Threats from Terrorism and Other Source, GAO-12-121, October 26, 2011; and Project
BioShield: Actions Needed to Avoid Repeating Past Problems with Procuring New Anthrax Vaccine and Managing the
Stockpile of Licensed Vaccine, GAO-08-88, October 23, 2007.
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Congress has also transferred funds from this account for various other purposes. The Omnibus
Appropriations Act, 2009 (P.L. 111-8) transferred $275 million to fund countermeasure advanced
development through the Biomedical Advanced Research and Development Authority (BARDA;
see “BioShield and BARDA” below) and $137 million to help respond to and prepare for
pandemic influenza.28 The Consolidated Appropriations Act, 2010 (P.L. 111-117) transferred $305
million to BARDA for countermeasure advanced development and $304 million to fund basic
research on biodefense and emerging infectious diseases at NIAID. In FY2011, the Department of
Defense and Full-Year Continuing Appropriations Act (P.L. 112-10) transferred $415 million to
BARDA for countermeasure advanced development.29 See Table 1.
The Consolidated Appropriations Act, 2010 (P.L. 111-117) transferred the remaining balance in
the DHS Biodefense Countermeasures account to the HHS Public Health and Social Services
Emergency Fund account. Congress specified that these transferred funds are to remain available
for obligation through FY2013 and to be used only for Project BioShield-related countermeasure
purchases. The Public Health and Social Services Emergency Fund account also contains non-
Project BioShield-related money designated for other purposes.
For FY2012, President Obama proposed transferring up to $765 million of Project BioShield
appropriated funds for other purposes. Of this amount, up to $665 million would have been
transferred for BARDA for countermeasure advanced development and administrative costs.30
The remaining $100 million of the requested transfer would have established an independent
medical countermeasure strategic investment corporation.31 In FY2012, the Consolidated
Appropriations Act, FY2012 (P.L. 112-74) transferred $415 million to BARDA for
countermeasure advanced development.32 Congress did not grant the Administration’s request for
a $100 million transfer to establish an independent medical countermeasure strategic investment
corporation.33
Acquisitions
The HHS awarded Project BioShield contracts for 10 different medical countermeasures. The
HHS has used Project BioShield to acquire countermeasures against only a few CBRN threats:
anthrax, smallpox, botulinum toxin, and radiological and nuclear threat agents. These
countermeasures include vaccines, antibodies, antivirals, and chemical compounds. Table 2
groups the Project BioShield countermeasures by threat and describes some of the details of the
contracts.
28 P.L. 111-8 explanatory statement, Congressional Record, February 23, 2009, p. H2240.
29 This amount includes funds transferred to BARDA through the earlier FY2011 continuing appropriations acts (P.L.
111-242, P.L. 111-290, P.L. 111-317, P.L. 111-322, P.L. 112-4, P.L. 112-6, and P.L. 112-8).
30 U.S. Department of Health and Human Services, Public Health and Social Services Emergency Fund Justification of
Estimates for Appropriations Committees FY2012, p. 49.
31 U.S. Department of Health and Human Services, Public Health and Social Services Emergency Fund Justification of
Estimates for Appropriations Committees FY2012, pp. 49 and 56.
32 U.S. Congress, House Committee on Appropriations, Military Construction and Veterans Affairs and Related
Agencies Appropriations Act, 2012, Conference Report to Accompany H.R. 2055, 112th Cong., 1st sess., December 15,
2011, H.Rept. 112-331 (Washington: GPO, 2011), p. 298.
33 The 112th Congress similarly rejected a FY2011 request to transfer $200 million from Project BioShield funds to
establish an independent medical countermeasure strategic investment corporation.
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The first Project BioShield contract was announced on November 4, 2004.34 The HHS contracted
with VaxGen, Inc., for delivery of 75 million doses of a new type of anthrax vaccine
(recombinant protective antigen or rPA) within three years. This contract had a value of $879
million. See Table 2. On December 17, 2006, HHS terminated this contract because VaxGen,
Inc., failed to meet a contract milestone.35 Subsequent contracts, grouped by threat agent, include:
• $691 million for 29 million doses of anthrax vaccine adsorbed (AVA), the
currently approved anthrax vaccine from Emergent BioSolutions, Inc.;
• $334 million for 65,000 doses of Raxibacumab (ABthrax), a treatment for
anthrax from Human Genome Sciences, Inc.;36
• $144 million for 10,000 doses of Anthrax Immune Globulin, a treatment for
anthrax from Cangene Corporation;
• $505 million for 20 million doses of Modified Vaccinia Ankara (MVA), a new
smallpox vaccine from Bavarian Nordic, Inc.;
• $433 million for 1.7 million doses of ST-246, an antiviral treatment for smallpox
from SIGA Technologies, Inc.;
• $414 million for 200,000 doses of botulinum antitoxin, a treatment for botulinum
toxin exposure from Cangene Corporation;
• $18 million for 5 million doses of a pediatric form of potassium iodide, a
treatment for radioactive iodine exposure from Fleming Pharmaceuticals; and
• $22 million for 395,000 doses of pentetate calcium trisodium (Ca-DTPA) and
80,000 doses of pentetate zinc trisodium (Zn-DTPA), two treatments for internal
radioactive particle contamination from Akorn, Inc.
Thus, excluding the canceled VaxGen contract, HHS has obligated approximately $2.56 billion to
date. Future targets for Project BioShield procurement include countermeasures against anthrax,
smallpox, viral hemorrhagic fevers, and radiation.37
As discussed above, HHS may add products lacking FDA approval to the Strategic National
Stockpile through Project BioShield. Raxibacumab (ABthrax), Anthrax Immune Globulin, MVA
smallpox vaccine, ST-246, and the botulinum antitoxin acquired through Project BioShield lack
FDA approval.
34 For the status of current requests and contracts, see the U.S. Department of Health and Human Services Project
BioShield procurement page at https://www.medicalcountermeasures.gov/BARDA/procurement/CBRN.aspx. For
issues regarding these awards, see CRS Report RL33907, Project BioShield: Appropriations, Acquisitions, and Policy
Implementation Issues for Congress, by Frank Gottron.
35 U.S. Department of Health and Human Services, “Termination Letter - Contract No. HHSO100200500001C,” Letter
to VaxGen, Inc., December 19, 2006.
36 This figure represents $326 million for the countermeasure and $8 million in additional payments for studies to
support FDA approval. HHS, personal communication with CRS, April 20, 2011.
37 U.S. Department of Health and Human Services, Public Health Emergency Medical Countermeasure Enterprise,
“Implementation Plan for Chemical, Biological, Radiological and Nuclear Threats,” 72 Fed. Reg. 20122, April 23,
2007; and U.S. Department of Health and Human Services, Public Health and Social Services Emergency Fund
Justification of Estimates for Appropriations Committees FY2012, pp. 57-63.
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Table 2. Project BioShield Acquisition Activity
Doses
Cost
Threat Product
(thousands)
($ millions)
Company
Award Date
11/4/04
Anthrax
rPA vaccine
75,000
879a VaxGen,
Inc.
Cancelled
12/19/06
Emergent
AVA vaccine
28,750
691
BioSolutions, Inc.
5/6/05; 5/5/06;
b
(formerly BioPort
9/25/07
Corp.)
Raxibacumab 65
334
6/19/06;
c
Human Genome
Sciences, Inc.
7/29/09
Anthrax Immune
10 144
Cangene
Corp. 7/28/06
Globulin
Smallpox
MVA vaccine
20,000
505
Bavarian Nordic, Inc.
6/4/07
ST-246 1,700
433
SIGA Technologies,
5/13/11
Inc.
Botulinum
Botulinum antitoxin
200
414d Cangene
Corp.
6/1/06
Toxin
Radiological/
3/18/05; 2/8/06
Nuclear
Potassium Iodide
4,800
18
Fleming
Pharmaceuticals
Ca-DTPA 395
22 Akorn,
Inc.
2/13/06
Zn-DTPA 80
Total Announced Obligations:
3,440
Total Current Obligations:
2,563e
Source: CRS analysis of HHS, Project BioShield: Annual Report to Congress July 2004-July 2006; HHS, Project
BioShield: Annual Report to Congress August 2006-July 2007; HHS, Project BioShield Annual Report to Congress August
2007 through December 2008; HHS, Project BioShield Annual Report to Congress January 2009-December 2009; DHS,
Office of Health Affairs, Biodefense Countermeasures Congressional Justification FY2010; HHS, “BARDA Supports
First Project BioShield Contract for Smal pox Drug,” press release, May 13, 2011; and personal communications
with HHS, June 8, 2009; December 29, 2010; April 20, 2011; and May 18, 2011.
a. This figure includes approximately $1.5 million that HHS paid to VaxGen, Inc. for mandatory security
upgrades. When HHS terminated the vaccine contract, VaxGen, Inc. kept this amount, while approximately
$877 million obligated for the vaccine became available for other Project BioShield procurements. Personal
communication with HHS, June 8, 2009.
b. This total does not include a $405 million contract for 14.5 million doses of AVA anthrax vaccine that HHS
announced on September 30, 2008. According to HHS, this contract used Centers for Disease Control and
Prevention funds rather than the Project BioShield special reserve fund. Personal communication with HHS,
June 8, 2009.
c. This figure includes $8 million in additional payments for studies to support FDA approval. Personal
communication with HHS, April 20, 2011.
d. This figure includes $50 million HHS obligated from the Project BioShield special reserve fund to this
company in FY2004 after the DHS Appropriations Act, 2004, funded this account but before passage of the
Project BioShield Act. See HHS, Project BioShield: Annual Report to Congress July 2004-July 2006, p. 31.
e. Announced awards minus $877 million for the cancelled rPA contract (see note a).
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BioShield and BARDA
Congressional policymakers have scrutinized the implementation and effectiveness of the Project
BioShield Act since its enactment. In response to perceived problems with medical
countermeasure development and acquisition, Congress created the Biomedical Advanced
Research and Development Authority (BARDA) through the Pandemic and All-Hazards
Preparedness Act (P.L. 109-417) in 2006.
Congress created in BARDA a dedicated infrastructure to manage and fund advanced
development and commercialization of CBRN countermeasures. As part of the Office of the HHS
Assistant Secretary for Preparedness and Response (ASPR), BARDA contracts with companies to
develop and commercialize countermeasures. These contracts specify development activities for
the company to perform and may extend multiple years. Congress funds this BARDA activity
through annual appropriations into the Biodefense Medical Countermeasure Development Fund.
The BARDA typically uses these funds to develop countermeasures not yet mature enough for a
Project BioShield acquisition contract.
The BARDA also manages and executes all Project BioShield acquisition contracts.38 Thus,
BARDA has two separate mechanisms to support countermeasure advanced development and
commercialization: countermeasure development contracts and Project BioShield acquisition
contracts with developmental milestone payments. In theory, HHS can now contribute to all
phases of a countermeasure’s development: basic research supported by NIAID, advanced
development and commercialization supported by BARDA, and acquisition supported by
BARDA and the Strategic National Stockpile (SNS). The Public Health and Emergency Medical
Countermeasure Enterprise, an interagency group headed by ASPR, is responsible for
coordinating these activities to ensure needs are addressed efficiently. The PHEMCE includes
members from FDA, CDC, NIH, DOD, DHS, the Department of Agriculture, and the Department
of Veterans Affairs.
Several groups, including the Institute of Medicine, the National Biodefense Science Board, and
GAO, have evaluated how these changes have affected federal efforts to develop and acquire
medical countermeasures. These studies determined that the creation of BARDA and PHEMCE
have helped, but that additional changes would further improve federal medical countermeasure
development and acquisition. These recommendations are discussed below in “Countermeasure
Development and Acquisition Process.”
Policy Issues and Options for Congress
As discussed above, the federal government has successfully used the Project BioShield Act
authorities to contribute to national preparedness for a CBRN attack and pandemic influenza.
However, questions remain on whether additional modifications to Project BioShield authorities
would improve their efficiency or performance and whether expiring authorities merit extension.
The 112th Congress is considering whether to reauthorize and modify the Project BioShield
38 Another part of ASPR, the Office of Policy and Planning, provides BARDA with specific countermeasure
requirements. U.S. Department of Health and Human Services, Public Health and Social Services Emergency Fund
Justification of Estimates for Appropriations Committees FY2012, p. 68.
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acquisition mechanism, whether to change the countermeasure development and acquisition
process, and whether to modify the authority to allow the emergency use of unapproved medical
countermeasures.
Project BioShield Acquisition Authority and Appropriations
The 10-year time period for which Congress funded Project BioShield acquisitions extends
through FY2013. As this date approaches, Congress may consider whether this procurement
mechanism merits reauthorizing and providing additional funding. Congressional policymakers
may determine that the program does not merit additional resources. Alternatively, congressional
policymakers may decide to extend the program as is or with modifications. If congressional
policymakers decide to extend the program, Congress may also change the amount appropriated
for these acquisitions.
Not Extend Project BioShield
Congressional policymakers could choose to let Project BioShield lapse for several reasons. One
reason could stem from the difficulty in determining how much safer Project BioShield has made
the nation. Most experts deem CBRN terrorist attacks as low probability events with a high
consequence. Thus, the federal government is unlikely to use medical countermeasures acquired
by Project BioShield. The medical countermeasures acquired through Project BioShield to date
provide protection against a limited number of all potential CBRN threats. The number of doses
acquired limits this potential protection to only a part of the population. Additionally, all of these
products expire. Maintaining each product’s potential benefit requires regular replacement, which
may add significant costs to the SNS budget.
Congressional policymakers could deem that the potential benefits provided by Project BioShield
do not justify continuing the program. Alternatively, policymakers could deem other, more
conventional, countermeasure procurement methods sufficient or more efficient than Project
BioShield and let it lapse. Finally, policymakers could decide that those funds could be better
used for other federal programs or not spent.
Extend Project BioShield
Policymakers considering extending the Project BioShield acquisition program will likely
consider how much to fund this program and for how long.
Funding Amount
By using the advanced appropriations mechanism to provide $5.6 billion to Project BioShield for
10 years, Congress anticipated an average annual obligation rate of $560 million. However
through FY2011, HHS obligated these funds at a slower pace, an average of $320 million
annually. Additionally, HHS could have purchased some of these products through other funding
sources, such as SNS appropriations. These factors might lead policymakers to decrease the
average annual appropriation for Project BioShield acquisitions.
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Since 2001, HHS has spent more than $15 billion on biodefense-related research and
countermeasure development.39 Congressional policymakers could determine that this investment
will begin producing more countermeasures in the near future. A potential increase in available
countermeasures might lead Congress to maintain or increase the average annual appropriation
for Project BioShield acquisitions.
Duration
In addition to determining the overall level of Project BioShield appropriations, congressional
policymakers may consider changing the method of providing appropriations. Previously,
Congress chose to advance appropriate funds for 10 years. Potential countermeasure developers
considered the establishment of a multiyear, advance-funded account dedicated solely to
countermeasure procurement as integral to their ability to develop countermeasures through this
program. The advance funding was to help assure developers that payment for successfully
developed countermeasures would not depend on future, potentially uncertain appropriations
processes. Although providing advance funding to the Project BioShield account may have
assured stable funding to developers, these funds have been subject to the annual appropriations
process. Subsequent Congresses have rescinded or transferred more than one-third of the advance
appropriation for other purposes. See Table 1.
Policymakers may choose to change how Project BioShield funds are appropriated to a traditional
single year at a time. However, developers continue to contend that a multiyear advance-funded
account devoted to Project BioShield acquisitions remains integral to their ability to develop
countermeasures.40 Additionally, annual appropriations may complicate HHS’s long-term
countermeasure development and acquisition planning. The inherent uncertainty in the
countermeasure development process produces uneven acquisition opportunities and activity. In
some years, one or multiple countermeasures may reach a point in development that HHS deems
appropriate for a Project BioShield contract. In those years, HHS might obligate hundreds of
millions of dollars for countermeasures. However, in years in which no countermeasures reach
that point in development, HHS might not obligate any money for Project BioShield contracts.
Policymakers may partially address some of these concerns by coupling annual appropriations
with allowing funds to remain available until expended.
Alternatively, Congress could use the advanced appropriations mechanism to provide funding for
multiple years as it did for FY2004-FY2013. This may address the developers’ desire for a
multiyear appropriation and may help HHS’s ability to plan acquisition programs. Developers
might prefer advance appropriations for as long a period as possible. However, providing a 10-
year advance appropriation for this program during the current fiscal environment may prove
more difficult than in 2003. Additionally, increasing the duration of the advance appropriation
may make it more likely that future Congresses transfer money out of the account for other
purposes. Congressional policymakers may decide to balance these competing pressures by
advance-appropriating funds for longer than 2 years but less than 10 years.
39 For one estimate, see Crystal Franco and Tara Kirk Sell, “Federal Agency Biodefense Funding, FY2011-FY2012,”
Biosecurity and Bioterrorism: Biodefense Strategy, Practice, and Science, vol. 9, no. 2 (2011), pp. 117-137.
40 U.S. Congress, House Committee on Appropriations, Subcommittee on Labor, Health and Human Services,
Education, and Related Agencies, Departments of Labor, Health and Human Services, Education, and Related
Agencies Appropriations for 2011, Part 6, Statements of Members of Congress and Other Interested Individuals and
Organizations, 111th Cong., 2nd sess., May 12, 2010 (Washington: GPO, 2010), pp. 197-204.
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The 112th Congress is considering extending the Project BioShield acquisition authority in H.R.
2405 and S. 1855.
Countermeasure Development and Acquisition Process
Project BioShield represents a piece of the federal effort to research, develop, and acquire
countermeasures for civilian use. Other aspects of this effort include risk assessment, strategic
planning, countermeasure prioritization, basic research, countermeasure approval, and
countermeasure distribution. Various federal agencies and departments have roles in different
parts of this effort.41 The Institute of Medicine and the National Biodefense Science Board
examined the federal government’s biodefense efforts and concluded that better coordination and
stronger management of the overall process would increase the pace of countermeasure
development and acquisition.42 Their report provided additional recommendations including
empowering a single office to have the authority and responsibility to align component agencies’
efforts; developing a coordinated budget request for HHS and DOD countermeasure
development, approval, and acquisition; developing a common set of prioritized product needs
and research goals to support them; and increasing the funding available for countermeasure
acquisition and advanced development.
In 2009, HHS Secretary Sebelius ordered a comprehensive review of how HHS develops and
acquires countermeasures to all public health threats, including CBRN agents.43 In August 2010,
HHS published the results of its review and recommendations.44
The review recommended creating a private strategic investment corporation to inject capital into
small companies developing novel technologies that could support public health needs and
medical countermeasure development.45 The HHS review modeled this corporation after In-Q-
Tel, a private corporation founded by the government to serve the needs of the intelligence
community.46 Congress did not grant President Obama’s FY2011 and FY2012 requests to transfer
money from the Project BioShield appropriation to initially fund the corporation ($200 million
and $100 million respectively).
41 For additional information, see CRS Report R41123, Federal Efforts to Address the Threat of Bioterrorism: Selected
Issues and Options for Congress, by Frank Gottron and Dana A. Shea.
42 Institute of Medicine, Board on Health Sciences Policy, The Public Health Emergency Medical Countermeasures
Enterprise Innovative Strategies to Enhance Products from Discovery Through Approval: Workshop Summary,
National Academies Press, 2010; and National Biodefense Science Board, Where Are the Countermeasures?
Protecting America’s Health from CBRN Threats, March 2010.
43 Secretary of Health and Human Services Kathleen Sebelius, remarks to The American Medical Association Third
National Congress on Health System Readiness, Washington, DC, December 1, 2009.
44 U.S. Department of Health and Human Services, Assistant Secretary for Preparedness and Response, The Public
Health Emergency Medical Countermeasures Enterprise Review: Transforming the Enterprise to Meet Long-Range
National Needs, August 2010.
45 For a description of HHS plans for this corporation, see U.S. Department of Health and Human Services, Public
Health and Social Services Emergency Fund Justification of Estimates for Appropriations Committees FY2012, p. 56.
46 Although analysts generally consider In-Q-Tel a success, other similar corporations established for other agencies
have been less successful. See Thomas J. Benjamin, Mary T. Tyszkiewicz, and Deborah Prigal, et al., Venture Capital
Concept Analysis Final Report, Homeland Security Institute, December 2005; and John M. Nolan, Emad U. Samad,
and Lawrence F. Jindra, et al., “Seeking Innovation: Incentive Funding for Biodefense Biotechs,” Biosecurity and
Bioterrorism: Biodefense Strategy, Practice, and Science, vol. 8, no. 4 (2010), pp. 365-372.
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The HHS review also recommended changing the medical countermeasure enterprise
management. The review determined that the HHS’s medical countermeasure decision-making
process would be improved by creating a centralized decision making body and by creating and
implementing a “disciplined, metric-driven, systematic” decision-making process.47 Additionally,
the review recommended the creation of a new position, the Medical Countermeasure (MCM)
Development Leader, to coordinate and integrate medical countermeasure development efforts
throughout the department. The review also determined that HHS should institute a five-year
budget planning system for medical countermeasure development activities. According to GAO,
HHS has made some progress implementing the reviews recommendations, but challenges
remain.48
The 112th Congress is considering these and other related policy options in H.R. 2405, S. 1855,
and H.R. 2356.
Emergency Use Authority
The Project BioShield Act provided the HHS Secretary with a mechanism to allow the emergency
use of unapproved countermeasures in certain circumstances. As noted above, HHS used this
authority several times. However, current legal restrictions on this authority may hinder
emergency planning and response.49 For example, the Secretary can only issue an EUA after
declaring an emergency. This creates some uncertainty for stakeholders developing response
plans about whether HHS will authorize the use of a particular countermeasure during a particular
emergency. The requirement for a declared emergency also complicates countermeasure pre-
positioning programs. Although HHS has used EUAs to allow two countermeasure prepositioning
programs, the FDA deems the EUA process too unwieldy to apply more broadly.50 Additionally,
many proposed methods of dispensing even FDA approved countermeasures during an
emergency would require an EUA. Modifying the EUA authority or specifically allowing
emergency dispensing of FDA approved countermeasures without a prescription might ease
federal, state, tribal, and local government planning activities and improve response during an
emergency.
The 112th Congress is considering several modifications to the emergency use authority in H.R.
2405 and S. 1855.
Current Legislation
The 112th Congress is considering legislation that would address some of these policy issues. Two
bills, the Pandemic and All-Hazards Preparedness Reauthorization Act of 2011 (H.R. 2405,
passed by the House on December 6, 2011) and the Pandemic and All-Hazards Preparedness
47 U.S. Department of Health and Human Services, Assistant Secretary for Preparedness and Response, The Public
Health Emergency Medical Countermeasures Enterprise Review: Transforming the Enterprise to Meet Long-Range
National Needs, August 2010, p. 17.
48 U.S. Government Accountability Office, National Preparedness: Improvements Needed for Acquiring Medical
Countermeasures to Threats from Terrorism and Other Sources, GAO-12-121, October 26, 2011.
49 H.Rept. 112-286, p. 25, and FDA personal communication with CRS, August 10, 2011.
50 FDA, personal communication with CRS, August 10, 2011.
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Reauthorization Act of 2011 (S. 1855, reported by the Senate Committee on Health, Education,
Labor, and Pensions on December 16, 2011), would extend the Project BioShield procurement
program, change the countermeasure development and acquisition process, and modify the
emergency use authority. A third bill, the WMD Prevention and Preparedness Act of 2011 (H.R.
2356, introduced on June 24, 2011), would change some aspects of the countermeasure
development and acquisition process.
H.R. 2405
The House passed the Pandemic and All-Hazards Preparedness Reauthorization Act of 2011
(H.R. 2405) on December 6, 2011. Some provisions of this bill would affect Project BioShield
implementation, address the use of the special reserve fund for purposes other than acquisition,
change the countermeasures development and acquisition process, and modify the emergency use
authority.
This bill would extend the Project BioShield procurement program to FY2018. It would authorize
appropriations of $2.8 billion for five fiscal years (FY2014-FY2018), the same average annual
appropriations as current law. It would also grant the HHS Secretary the authority to use up to
$840 million of Project BioShield appropriations for BARDA countermeasure advanced
development activities. The HHS Secretary would have to report to Congress when the special
reserve fund available balance dropped below $1.5 billion.
H.R. 2405 would also change the countermeasure development and acquisition process by
reauthorizing BARDA and requiring formal planning activities and reporting. The bill would
authorize $415 million in annual appropriations for BARDA countermeasure development
activities through FY2016, in addition to any funds transferred from the BioShield special reserve
fund. Additionally, it would require the HHS Assistant Secretary for Preparedness and Response
(ASPR) to develop a “comprehensive cross-cutting 5-year budget analysis” for its
countermeasure advanced research, development, and procurement activities. H.R. 2405 would
require the ASPR to develop an annual Countermeasure Implementation Plan that would be
provided to Congress. The plan must describe the CBRN threats; describe the efforts to develop
countermeasures for each threat; evaluate the progress of all activities to develop, procure,
stockpile, deploy, and use countermeasures; identify and prioritize near-term, mid-term, and long-
term needs; summarize all advanced development and procurement awards; provide timelines,
metrics, and intended uses for each countermeasure under development; evaluate progress on all
such awards; report the amount available in the BioShield fund; incorporate stakeholder input;
and address the need for pediatric countermeasures. H.R. 2405 would also repeal the reporting
requirements section of the Project BioShield Act discussed above (“Reporting Requirements”).
H.R. 2405 would modify some aspects of the HHS emergency use authority for medical
countermeasures. In the public health context, current law requires that an emergency actually
exist before the Secretary issues an EUA. In contrast, EUAs may be issued on the basis of a
potential military or domestic emergency. H.R. 2405 would allow the Secretary to issue an EUA
following the determination that a significant potential for a public health emergency exists.
EUAs would expire when the HHS Secretary determines the underlying emergency
circumstances no longer exist rather than automatically after one year. H.R. 2405 would also
allow the Secretary to modify active EUAs and waive certain manufacturing process
requirements for approved products during an emergency. It would allow mass dispensing of
approved medical countermeasures during an emergency without an individual prescription
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(independent of an EUA) and pre-positioning of unapproved medical countermeasures by federal,
state, or local governments in anticipation of emergencies.
S. 1855
The Senate Committee on Health, Education, Labor, and Pensions reported the Pandemic and All-
Hazards Preparedness Act Reauthorization of 2011 (S. 1855) on December 16, 2011. This bill
would address several Project BioShield-related policy issues. Some of the provisions of this bill
would affect Project BioShield implementation, address the use of the special reserve fund for
purposes other than acquisition, change the countermeasures development and acquisition
process, and modify the emergency use authority.
This bill would extend the Project BioShield procurement program to FY2018. It would authorize
appropriations of $2.8 billion for five fiscal years (FY2014-FY2018), the same average annual
appropriations as current law. The HHS Secretary would have to report to Congress when the
special reserve fund available balance dropped below $1.5 billion. In contrast to H.R. 2405, it
would not authorize the Secretary to use the Project BioShield special reserve fund to support
BARDA countermeasure development activities. It would explicitly allow Project BioShield
countermeasure procurement contracts to include development costs. Additionally, it would allow
Project BioShield contracts to be signed up to 10 years before the expected delivery date of the
countermeasure to the stockpile, rather than the 8 years under current law.
S. 1855 would also reauthorize BARDA and require formal planning activities and reporting. The
bill would authorize $415 million in annual appropriations to BARDA for countermeasure
development activities through FY2016. S. 1855 would require the ASPR to develop a biennial
“Public Health and Emergency Medical Countermeasures Enterprise Strategy and
Implementation Plan.” This plan must consider and reflect all CBRN-countermeasure-related
activities, including basic research, development, procurement, stockpiling, deployment, and
distribution; identify and prioritize near-term, mid-term, and long-term needs; identify projected
timelines, funding, benchmarks, and milestones for each countermeasure; be informed by
National Biodefense Science Board recommendations; report on advanced research and
development awards; report on BioShield contracts; identify progress in meeting goals,
benchmarks, and milestones; and be publically available. Additionally, the HHS Secretary would
be required to develop and annually update a coordinated five-year budget plan for all activities
related to the Public Health and Emergency Medical Countermeasures Enterprise Strategy and
Implementation Plan. This plan must identify countermeasure life-cycle costs and include
measurable outputs and outcomes to track progress towards meeting needs. This plan would be
made available to the appropriate congressional committees.
S. 1855 would modify some aspects of the HHS emergency use authority for medical
countermeasures. Similar to H.R. 2405, S. 1855 would allow the Secretary to issue an EUA
following the determination that a significant potential for a public health emergency exists.
EUAs would expire when the HHS Secretary determines the underlying emergency
circumstances no longer exist rather than automatically after one year as under current law. Also
like H.R. 2405, S. 1855 would allow the Secretary to modify active EUAs; waive certain
manufacturing process requirements for approved products during an emergency; and allow pre-
positioning of unapproved medical countermeasures by federal, state, or local governments in
anticipation of emergencies. However, unlike H.R. 2405, S. 1855 would allow the Secretary to
issue an EUA on the basis of a material threat determination by DHS, a designation required for
all medical countermeasures acquired through Project BioShield.
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The Project BioShield Act: Issues for the 112th Congress
H.R. 2356
The WMD Prevention and Preparedness Act of 2011 (H.R. 2356) was introduced June 24, 2011.
This bill would change the countermeasure development and acquisition process. This bill was
referred to the House Committees on Homeland Security, Energy and Commerce, Transportation
and Infrastructure, Foreign Affairs, and Intelligence. None of the committees has ordered this bill
reported.
H.R. 2356 would create a new White House position to coordinate federal biodefense policy and
require new formal planning activities and reporting. This bill would require the President to
appoint a Special Assistant to the President for Biodefense. This person would be the principal
advisor to the President on coordination of federal biodefense policy, be responsible for
developing several federal biodefense-related plans, and conduct oversight and evaluation of
federal biodefense activities.
The Special Assistant to the President for Biodefense would lead the development of a National
Biodefense Plan that would include prevention, protection, response, and recovery activities. This
plan would identify which biological risks facing the nation should be addressed; delineate the
activities to be performed to address these risks; identify biodefense assets and capability gaps;
define organizational roles, responsibilities, and coordination of federal, state, local, and tribal
authorities; and incorporate input from stakeholders. This report would be delivered to the
President and Congress 18 months after enactment and updated as necessary.
The Special Assistant to the President for Biodefense would also lead the development of an
annual cross-cutting biodefense budget analysis. This submission would include detailed account
level amounts for biodefense activities and how these activities support the National Biodefense
Plan. This analysis would include biodefense budgets of the Departments of Agriculture,
Commerce, Defense, Energy, Health and Human Services, Homeland Security, State, Veterans
Affairs, Justice, and the Environmental Protection Agency, National Science Foundation, and the
United States Postal Service.
Author Contact Information
Frank Gottron
Specialist in Science and Technology Policy
fgottron@crs.loc.gov, 7-5854
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