PREVENT Pandemics Act (P.L. 117-328, Division FF, Title II)

August 15, 2023 R47649

PREVENT Pandemics Act (P.L. 117-328, Division August 15, 2023
FF, Title II)
Kavya Sekar, Coordinator
The Prepare for and Respond to Existing Viruses, Emerging New Threats, and Pandemics Act
Analyst in Health Policy
(PREVENT Pandemics Act) was enacted on December 29, 2022, as a part of Consolidated

Appropriations Act, FY2023 (CAA, P.L. 117-328; Division FF; Title II). The act marks the first
set of cross-cutting legislative reforms to address pandemic preparedness and response policy

after the Coronavirus Disease 2019 (COVID-19) pandemic began. The law also addresses other
issue areas with implications for pandemic preparedness and response, such as those related to general public health, medical
supply chains, biomedical innovation, and research security.
The PREVENT Pandemics Act addresses mostly programs and agencies of the Department of Health and Human Services
(HHS), especially some of the HHS agencies involved in pandemic preparedness and response, including the Centers for
Disease Control and Prevention (CDC), the Administration for Strategic Preparedness and Response (ASPR, formerly Office
of the Assistant Secretary for Preparedness and Response), the National Institutes of Health (NIH), and the U.S. Food and
Drug Administration (FDA). The PREVENT Pandemics Act also establishes a new White House Office of Pandemic
Preparedness and Response Policy to coordinate pandemic preparedness and response activities across the federal
government.
A version of the PREVENT Pandemics Act (S. 3799) was passed by the Senate Committee on Health, Education, Labor, and
Pensions in March 2022. With some changes from the Senate committee-passed bill, the PREVENT Pandemics Act was
ultimately incorporated into the CAA (P.L. 117-328) alongside other health policy provisions. In summary, the subtitles of
the PREVENT Pandemics Act focus on the following:
• Strengthening Federal and State Preparedness. Subtitle A addresses the roles and responsibilities of
federal agencies and offices involved in pandemic preparedness and response, including CDC, ASPR, and
the new White House Office of Pandemic Preparedness and Response. The subtitle also addresses state-
level preparedness for infectious disease emergencies.
• Improving Public Health Preparedness and Response Capacity. Subtitle B addresses several public
health issues related to the pandemic, including public health data sharing and modernization, health
disparities, public health workforce programs, and other specific programs related to infectious diseases
and emergency response.
• Accelerating Research and Countermeasure Discovery. Subtitle C addresses federal scientific and
research and development (R&D) programs related to pandemic pathogens and other biological threats.
The subtitle focuses in large part on research security issues, including laboratory biosafety and biosecurity,
foreign influence, and the protection of sensitive or proprietary data and information in research. This
subtitle also includes authorization for the new Advanced Research Projects Agency for Health (ARPA-H),
an agency focused on high-risk, high-reward health research that was first funded in 2022.
• Modernizing and Strengthening the Supply Chain for Vital Medical Products. Subtitle C focuses on
medical supply availability and distribution during public health emergencies. Several provisions in the
subtitle address the Strategic National Stockpile, the federal stockpile of medical products maintained by
ASPR for bioterrorist attacks and other public health emergencies. Provisions also address state stockpiles
as well as programs and incentives for domestic manufacturing of critical medical products, such as generic
medicines and antibiotics.
• Enhancing Development and Combating Shortages of Medical Products. Subtitle E addresses FDA’s
role in pandemic preparedness and response. First, the subtitle addresses FDA’s review and regulation of
medical products for emergencies. Second, the subtitle addresses FDA’s role in mitigating medical product
shortages and ensuring the quality of the U.S. medical supply chain.
This CRS report provides a section-by-section overview of the PREVENT Pandemics Act. The report is organized by subtitle
of the act and includes general background followed by a summary of each provision.
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PREVENT Pandemics Act (P.L. 117-328, Division FF, Title II)

Introduction
The Prepare for and Respond to Existing Viruses, Emerging New Threats, and Pandemics Act
(PREVENT Pandemics Act) was enacted on December 29, 2022, as a part of the Consolidated
Appropriations Act, 2023 (P.L. 117-328; Division FF; Title II). The act marks the first set of
cross-cutting legislative reforms to address pandemic preparedness and response policy after the
Coronavirus Disease 2019 (COVID-19) pandemic began. The law also addresses other issue
areas with implications for pandemic preparedness and response, such as those related to general
public health, medical supply chains, biomedical innovation, and research security.
The PREVENT Pandemics Act addresses Department of Health and Human Services (HHS)
programs, especially those of the key HHS agencies involved in pandemic preparedness and
response, including the Centers for Disease Control and Prevention (CDC), the Administration for
Strategic Preparedness and Response (ASPR, formerly Office of the Assistant Secretary for
Preparedness and Response), the National Institutes of Health (NIH), and the U.S. Food and Drug
Administration (FDA). The PREVENT Pandemics Act also establishes a new White House
Office of Pandemic Preparedness and Response Policy to coordinate pandemic preparedness and
response activities across the federal government.
A version of the PREVENT Pandemics Act (S. 3799) was first passed by the Senate Committee
on Health, Education, Labor, and Pensions (HELP) in March 2022. According to the press release
following the committee vote, the bill incorporated ideas from 41 different bills and 35 different
Senators.1 Regarding issues addressed by the bill, the press release stated,
[The COVID-19 pandemic] has also put a harsh spotlight on some of the longstanding
challenges the United States’ public health preparedness systems face and brought to light
unanticipated challenges. Broken supply chains and inadequate stockpiles led to shortages
of masks, ventilators, and other medical products. Tests throughout the response have been
either critically delayed or scarce, leaving workers, schools, and communities unable to
make informed, timely decisions about how to keep themselves and those around them
safe. Outdated and inconsistent public health data systems made it hard for federal, state,
local, Tribal and territorial public health departments to get a full picture of the crisis and
inform their responses. The nation’s public health and health care workforce was
overwhelmed. Mental health and substance use disorder challenges and health disparities,
which were already damaging to so many communities, worsened during this crisis.
With some changes from the Senate committee-passed bill, the PREVENT Pandemics Act was
ultimately incorporated into the Consolidated Appropriations Act, 2023 (P.L. 117-328) in
Division FF, alongside many other health policy provisions.
The PREVENT Pandemics Act is a separate legislative effort from reauthorization of the
Pandemic and All-Hazards Preparedness Act (PAHPA). Some provisions of the PREVENT
Pandemics Act address programs that have historically been included in PAHPA reauthorizations,
such as CDC’s public health emergency preparedness and biosurveillance programs, the Strategic
National Stockpile, and other ASPR programs. However, with some exceptions, the PREVENT
Pandemics Act made no changes to expiration dates from the last PAHPA reauthorization, the
Pandemic and All-Hazards Preparedness and Advancing Innovation Act of 2019 (PAHPAIA; P.L.

1 Senate Committee on Health, Education, Labor, and Pensions (HELP), “HELP Committee Passes Murray-Burr
PREVENT Pandemics Act In Overwhelming Bipartisan Vote,” press release, March 15, 2022,
https://www.help.senate.gov/chair/newsroom/press/help-committee-passes-murray-burr-prevent-pandemics-act-in-
overwhelming-bipartisan-vote.
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PREVENT Pandemics Act (P.L. 117-328, Division FF, Title II)

116-22), including many expiration dates in 2023. Thus, House and Senate committees have
considered PAHPA reauthorization bills in 2023.2
In addition, the PREVENT Pandemics Act addresses programs and issues that have not
historically been addressed in past PAHPA reauthorizations, including CDC agency-wide
leadership and strategic planning, foreign influence in HHS biomedical research, medical product
shortages, and general public health programs and data sharing. The law includes formal
authorization for the new Advanced Research Projects Agency for Health (ARPA-H), an agency
focused on high-risk, high-reward health research that was first funded in 2022.3
This CRS report provides a section-by-section overview of the PREVENT Pandemics Act. The
report is organized by subtitle of the act and includes general background followed by a summary
of each provision.
The PREVENT Pandemics Act: At a Glance
In summary, the subtitles of the PREVENT Pandemics Act focus on the following:
• Strengthening Federal and State Preparedness. Subtitle A addresses the roles
and responsibilities of federal agencies and offices involved in pandemic
preparedness and response, including CDC, ASPR, and the new White House
Office of Pandemic Preparedness and Response. The subtitle also addresses state-
level preparedness for infectious disease emergencies.
• Improving Public Health Preparedness and Response Capacity. Subtitle B
addresses several public health issues related to the pandemic, including public
health data sharing and modernization, health disparities, public health workforce
programs, and other specific programs related to infectious diseases or
emergency response.
• Accelerating Research and Countermeasure Discovery. Subtitle C addresses
federal scientific and research and development (R&D) programs related to
pandemic pathogens and other biological threats. The subtitle focuses in large
part on research security issues, including laboratory biosafety and biosecurity,
foreign influence, and the protection of sensitive or proprietary data and
information in research. This subtitle includes authorization for the new
Advanced Research Projects Agency for Health (ARPA-H), an agency focused
on high-risk, high-reward health research that was first funded in 2022.
• Modernizing and Strengthening the Supply Chain for Vital Medical
Products. Subtitle D focuses on medical supply availability and distribution
during public health emergencies. Several provisions in the subtitle address the
Strategic National Stockpile, the federal stockpile of medical products
maintained by ASPR for bioterrorist attacks and other public health emergencies.
Provisions also address state stockpiles as well as programs and incentives for

2 U.S. Senate HELP Committee, "S. 2333, Pandemic and All-Hazards Preparedness and Response Act," press release,
July 20, 2023, https://www.help.senate.gov/hearings/s-2333-pandemic-and-all-hazards-preparedness-and-response-act,
and House Energy and Commerce Committee, "Health Subcommittee Chair Guthrie Opening Statement at
Subcommittee Markup of 17 Bills," press release, July 13, 2023, https://energycommerce.house.gov/posts/health-
subcommittee-chair-guthrie-opening-statement-at-subcommittee-markup-of-17-bills.
3 See CRS Report R47074, Advanced Research Projects Agency for Health (ARPA-H): Congressional Action and
Selected Policy Issues.
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domestic manufacturing of critical medical products, such as generic medicines
and antibiotics.
• Enhancing Development and Combating Shortages of Medical Products.
Subtitle E addresses FDA’s role in pandemic preparedness and response. First,
the subtitle addresses FDA’s review and regulation of medical products for
emergencies. Second, the subtitle addresses FDA’s role in mitigating shortages of
medical products and ensuring the quality of the U.S. medical supply chain.
The PREVENT Pandemics Act is an authorizing law; it does not appropriate any funds. Some of
the existing programs addressed in the law have not been funded in recent years. It remains to be
seen whether new programs established by the law will be funded through future appropriations.
In this report, “Secretary” means “HHS Secretary” unless otherwise specified.
Subtitle A—Strengthening Federal and State
Preparedness
Chapter 1—Federal Leadership and Accountability
Under the National Response Framework, HHS is the primary agency responsible for the public
health and medical aspects of federal preparedness and response to emergencies.4 Within HHS,
the Assistant Secretary for Preparedness and Response is established by statute as the principal
advisor to the HHS Secretary on federal public health and medical preparedness and response.5
The Assistant Secretary leads the Administration for Strategic Preparedness and Response
(ASPR), an HHS operating division that has significant responsibilities for leading public health
emergency responses. However, other HHS agencies also play a major role in health emergency
response. In particular, CDC has responsibilities and expertise related to controlling infectious
diseases and responding to outbreaks. During the COVID-19 pandemic, some uncertainties arose
around the respective roles of ASPR and CDC and their relationship with other federal agencies
in the response.6 In addition, many have called into question CDC’s preparedness for and
leadership during the pandemic; the agency itself has acknowledged a need for reform.7 In 2021,
the Government Accountability Office (GAO) added HHS’s leadership and coordination of public
health emergencies to its list of high-risk issue areas in need of reform.8

4 See Federal Emergency Management Agency, “Emergency Support Function #8 – Public Health and Medical
Services Annex,” https://www.fema.gov/sites/default/files/2020-07/fema_ESF_8_Public-Health-Medical.pdf.
5 PHSA Section 2811.
6 See, for example, U.S. Government Accountability Office (GAO), COVID-19: HHS Should Clarify Agency Roles for
Emergency Return of U.S. Citizens during a Pandemic, GAO-21-334, April 19, 2021, https://www.gao.gov/products/
gao-21-334.
7 See, for example, Senator Burr, “Modernizing CDC: Ensuring a Strategic Approach and Improving Accountability,”
May 2021, https://www.help.senate.gov/imo/media/doc/Modernizing%20CDC%20-
%20Ensuring%20a%20Strategic%20Approach%20and%20Improving%20Accountablity.pdf, and Jeneen Interlandi,
“Covid Proved the C.D.C. Is Broken. Can It Be Fixed?,” The New York Times, June 16, 2021. On agency reform, see
CDC, “CDC Moving Forward,” https://www.cdc.gov/about/organization/cdc-moving-forward.html.
8 GAO, High-Risk Series: Efforts Made to Achieve Progress Need to Be Maintained and Expanded to Fully Address All
Areas, GAO-23-106203, April 20, 2023, https://www.gao.gov/products/gao-23-106203.
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Sections 2101: Appointment and authority of the Director of the Centers for
Disease Control and Prevention
Background
CDC, the federal government’s focal point for disease prevention and control activities, was
established administratively as funded by appropriations.9 CDC comprises several centers,
institutes, and offices (CIOs) that focus on a wide array of health topics, including infectious
diseases, noninfectious diseases, injury, disability, occupational health, environmental health, and
public health emergency preparedness and response. In addition, CDC oversees the Agency for
Toxic Substances and Disease Registry (ATSDR), a separate HHS operating division.10 Many of
CDC’s programs are based in general authorities in the Public Health Service Act (PHSA).11 CDC
has periodically developed agency-wide strategic plans, such as for 2022 to 2027.12 Prior to the
PREVENT Pandemics Act, neither the position of the CDC Director nor the requirement for a
strategic plan was explicitly authorized in statute.
Provision
Section 2101 adds a new PHSA Section 305 to PHSA Title III, where many CDC authorities,
including to collect data and to award public health grants, are currently based. The new section
does three things:
First, PHSA Section 305 codifies the position of the CDC Director as a presidentially appointed
and Senate-confirmed position, which becomes effective on January 20, 2025. The section also
formally authorizes the CDC Director’s role as Administrator of ATDSR. PHSA Section 305 tasks
the CDC Director with exercising authorities and responsibilities related to public health both
domestically and globally, including the prevention and control of diseases, as well as addressing
injuries and occupational and environmental hazards. The section also makes the Director
responsible for (1) the overall direction and management of the agency, (2) coordination among
CDC CIOs, (3) overseeing strategic planning and performance, and (4) communicating the
strategic plan and CDC’s programs to public and private stakeholders, including through annual
meetings. PHSA Section 305 also requires the Director to appear at hearings before specified
congressional committees each fiscal year to address topics related to public health emergency
preparedness and planning.
Second, PHSA Section 305 establishes requirements for CDC’s strategic plan. One year after
enactment, and every four years after, the CDC Director is required to submit a strategic plan to
specified congressional committees and to post the plan online. The strategic plan must identify
priorities and objectives related to (1) preventing, reducing, and eliminating communicable and
noncommunicable diseases or conditions and addressing injuries and occupational and
environmental hazards; (2) supporting state, local, territorial, and tribal (SLTT) health
departments in these efforts; (3) containing, mitigating, and ending disease outbreaks; (4)
enhancing global and domestic public health capacity, including public health data, surveillance,
workforce, and laboratory capacity; and (5) other priorities identified by the Director. The plan
must describe the capacity and capabilities needed to achieve identified priorities, as well as

9 Elizabeth W. Etheridge, Sentinel for Health: A History of the Centers for Disease Control and Prevention (University
of California Press, 1992), pp. 16-17.
10 CDC, “Official Organizational Chart,” February 2023, https://www.cdc.gov/about/pdf/organization/cdc-org-
chart.pdf.
11 See CRS In Focus IF12241, The Centers for Disease Control and Prevention (CDC).
12 See, CDC, “CDC’s 2022-2027 Strategic Plan: Advancing Science and Health Equity,” https://www.cdc.gov/about/
strategic-plan/index.html.
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progress made in achieving such capacity and capabilities. The plan must also incorporate
descriptions related to strategic communications; partnerships with private and public sector
entities, including SLTT public health departments; and coordination with other HHS and federal
agencies. Strategic plans of CDC CIOs are to be prepared regularly and informed by the CDC-
wide strategic plan.
Third, PHSA Section 305 provides CDC with Other Transactions (OT) authority for infectious
disease research, biosurveillance, infectious disease modeling, and public health preparedness and
response. An OT is not a contract, grant, or cooperative agreement, and there is no one statutory
or regulatory definition of “other transaction.” Typically, OT authority gives agencies more
flexibility for engaging with private industry and other partners than allowed under regular
federal funding awards (e.g., grants, contracts).13 The new authority specifies conditions for
making awards over $40 million and requires that CDC establish guidelines for using OT
authority that include auditing requirements.
Section 2102: Advisory Committee to the Director of the Centers for Disease
Control and Prevention
Background
From time to time, CDC has established under general authority an Advisory Committee to the
Director of the Centers for Disease Control and Prevention. The committee is composed of
nonfederal experts to advise on overall CDC policy and strategy. Most recently, CDC
reestablished the committee in 2021.14
Provision
This provision adds a new PHSA Section 305A, which codifies a requirement to establish the
Advisory Committee to the Director to advise the CDC Director on policies and strategy to
achieve CDC’s mission. The Advisory Committee is to be made up of 15 nonfederal members, 12
of whom are to be representatives of health disciplines relevant to CDC. Three members may be
appointed from the general public and may include leaders in innovation, public policy, public
relations, law, economics, or management.
The Advisory Committee is allowed to (1) advise on development of the strategic plan; (2) make
recommendations regarding prioritizing agency activities in alignment with its strategic plan; (3)
advise on ways to improve performance; (4) advise on funding awards like grants, cooperative
agreements, contracts, and other transactions; (5) advise on CDC activities related to research,
surveillance, and support to SLTT public health departments; and (6) appoint subcommittees.
Section 2103: Public health and medical preparedness and response
coordination
Background

13 See, for example, CRS Report R45521, Department of Defense Use of Other Transaction Authority: Background,
Analysis, and Issues for Congress.
14 CDC, “Advisory Committee to the Director,” https://www.cdc.gov/about/advisory-committee-director/index.html
and HHS, “Charter: Advisory Committee to the Director, Centers for Disease Control and Prevention,”
https://www.cdc.gov/about/advisory-committee-director/pdf/HHS-2021-charter-signed_4.15.21.pdf.
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The HHS Secretary has the authority to declare a public health emergency at his or her discretion
under conditions dictated under PHSA Section 319.15 Additional authorities and responsibilities
related to public health emergency response are also detailed in this PHSA section, including the
use of the Public Health Emergency Fund (PHEF). The PHEF is an emergency reserve fund
available for PHEs (or expected PHEs) authorized in PHSA Section 319. The PHEF has not
received appropriations in many years and has a balance of $56,500 as of July 2023.16
PHSA Title XXVIII defines HHS responsibilities for preparedness and response to public health
emergencies. Within this title, the position of the Assistant Secretary for Preparedness and
Response is established in PHSA Section 2811 as the principal advisor to the HHS Secretary on
federal public health and medical preparedness and response. As mentioned earlier, the Assistant
Secretary leads the Administration for Strategic Preparedness and Response (ASPR).17 The duties
of the ASPR include (1) providing leadership at the federal level for public health and medical
preparedness and response; (2) developing and procuring advanced medical countermeasures
(MCM), medical products that can be used to diagnose, prevent, or treat diseases related to
chemical, biological, radiological, or nuclear (CBRN) threats; (3) coordinating activities, policies,
and operations among and within different levels of government during responses; and (4)
assessing threats to maintain preparedness and situational awareness for public health security.18
Provision
This provision contains several sections aimed at improving aspects of public health and medical
preparedness and response coordination. Specifically, the provision amends PHSA sections as
follows:
• Amends PHSA Section 319(b) to allow Public Health Emergency Fund (PHEF)
funds to be used to support the initial deployment and distribution of SNS
contents, and requires the HHS Secretary to report to Congress on expenditures
from the PHEF each fiscal year as specified.19
• Amends PHSA Section 2801 to require that the HHS Secretary coordinate with
other federal departments and agencies to carry out necessary public health and
medical response activities to support the public health and medical response for
SLTT agencies.20
• Amends PHSA Section 2811(b) to clarify the roles and responsibilities of the
Assistant Secretary in public health and medical response to public health
emergencies.21 These amendments clarify that the Assistant Secretary is to assist
the HHS Secretary in leading public health and medical response to public health
emergencies consistent with the National Response Framework and other
applicable provisions of law. This provision also directs the Assistant Secretary to
conduct annual drills and operational exercises, including national-level and

15 42 U.S.C. §247d.
16 USASpending, “Public Health Emergency Fund,” accessed July 1, 2023, https://www.usaspending.gov/
federal_account/075-1104.
17 Formerly the Office of the Assistant Secretary for Preparedness and Response, the office was renamed and
reestablished as an HHS operating division, the Administration for Strategic Preparedness and Response, effective
February 2023. See 88 Federal Register 10125.
18 PHSA Section 2811(b).
19 42 U.S.C. §247d(b).
20 42 U.S.C. §300hh.
21 42 U.S.C. §300hh-10(b).
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state-level, full-scale exercises at least once every four years. Such exercises are
to assess the ability of the Strategic National Stockpile (see “Strategic National
Stockpile: Sections 2402-240” for background) to provide MCMs and supplies in
response to a PHE (including during a large-scale, long-term response) in
coordination with state and local officials.
• Amends PHSA Section 2811(b) to further require the Assistant Secretary to
coordinate HHS efforts to plan for medical product and supply needs in CBRN
and other emergency responses.
• Amends PHSA Title Section 2811(b) by adding a requirement that the ASPR
appear annually before Congress to report on various aspects of public health
emergency preparedness and medical response.22
• Amends PHSA Title Section 2801 to direct the HHS Secretary produce an annual
report to Congress containing information on assessments of any PHE response;
findings related to drills and exercises; the state of CBRN preparedness and
response; and any challenges.23
Lastly, this provision directs GAO to issue two reports within three years after enactment. For the
first report, GAO is to review previous and current interagency agreements between the HHS
Secretary and the heads of other federal departments or agencies involved in public health and
medical emergency responses.24 GAO is to examine several aspects of these agreements,
including specific roles and responsibilities of each entity, how frequently these agreements were
utilized, gaps or barriers to establishing or implementing these agreements, and recommendations
on how to improve these agreements. For the second report, GAO is to review how the HHS
Secretary has implemented and utilized the new authority to coordinate with other federal
agencies for public health responses as added by Section 2103.25
Section 2104: Office of Pandemic Preparedness and Response Policy
Background
The Executive Office of the President, created in 1939, provides support to the President in a
number of policy areas. Existing subdivisions of the Executive Office include the Domestic
Policy Council, the National Security Council, and the Office of Management and Budget, among
many others.26 At times, positions within the White House have been dedicated to biodefense and
pandemic preparedness; however, such positions were established at the discretion of Presidents
and have not been required by statute.27
Provision
This provision establishes within the Executive Office of the President a new Office of Pandemic
Preparedness and Response Policy. This office is to be headed by a Director appointed by the
President. The functions of the Director include serving as the principal advisor to the President

22 Ibid.
23 42 U.S.C. §300hh.
24 Ibid.
25 42 U.S.C. §300hh(c) as introduced by the PREVENT Pandemic Act.
26 The White House, Executive Office of the President, https://www.whitehouse.gov/administration/executive-office-of-
the-president/.
27 For general background, see Gail Wilensky, “The Importance of Reestablishing a Pandemic Preparedness Office at
the White House,” Journal of the American Medical Association, vol. 1, no. 7 (July 9, 2020).
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on all matters related to preparedness and response to pandemics and other biological threats;
coordinating federal activities to prepare for and respond to these threats as specified; promoting
the development of expertise within the federal government to ensure that the United States can
detect, identify, and respond to these threats; consulting with relevant officials within the
Executive Office of the President on preparedness and response activities; and identifying
opportunities to leverage current and emerging technologies, and ensuring that federal after-
action report (AAR) findings are implemented. The Director is to also lead an interdepartmental
working group and appoint an Industry Liaison during a pandemic response.
In addition, the Director is directed to publish several reports:
• Within a year of its operation and in consultation with relevant federal agencies,
the Director is required to publish a report on conditions that warrant special
attention within the next five years involving current and emerging problems
related to pandemics or other biological threats, and that discusses opportunities
for developing and procuring MCMs. The report is to be revised at least once
every five years.
• Within 18 months of enactment of PREVENT and every two years thereafter, the
office is directed to issue a report to the President and Congress on current
emerging threats, roles, and responsibilities of the federal government; findings
of the preceding review; barriers to addressing such findings; and current and
planned activities to update federal policies, strategies, and procedures, and to
support the development of federal expertise and improve federal preparedness
and response capabilities using emerging technologies.
Lastly, this provision requires the Director to conduct a review of federal strategies, policies,
procedures, and AARs to identify pandemic preparedness and response gaps and inefficiencies
within one year of enactment of the PREVENT Pandemics Act.
Chapter 2—State and Local Readiness
State, local, tribal and territorial (SLTT) jurisdictions play a significant role in preparing for and
responding to emergencies. SLTT agencies are responsible for a range of activities, including
developing incident response plans in anticipation of emergencies; coordinating with local
stakeholders to enhance response efforts; executing training, exercises, and drills to develop
emergency response skillsets; and implementing emergency response plans during emergency
incidents.28 A variety of federal programs, grants, and guidance are available to assist jurisdictions
in their preparedness and response efforts. This chapter focuses on enhancing the ability of SLTT
to prepare for and respond to future public health emergencies.
Section 2111: Improving State and local public health security
Background
The Public Health Emergency Preparedness (PHEP) cooperative agreement program is
administered by the CDC as authorized in PHSA Section 319C-1.29 Funding is provided
according to a statutory formula to 62 grantees, comprising all 50 states, the District of Columbia,

28 FEMA, “How Communities and States Deal with Emergencies and Disasters,” p. 2, https://training.fema.gov/
emiweb/downloads/is7unit_2.pdf.
29 CDC, “Public Health Emergency Preparedness Program and Guidance,” https://www.cdc.gov/orr/readiness/phep/
index.htm.
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five territories, three freely associated states, and three major localities: New York City, Los
Angeles County, and Chicago.30 Funds distributed through the agreement are a source of funding
for public health departments to bolster their ability to prepare for and respond to a variety of
emergencies.31 Eligible grantees must submit an application as specified by statute.32
Provision
This provision contains a number of amendments to PHSA Section 319C-1, which lists the
requirements eligible entities must demonstrate when applying for the PHEP cooperative
agreement.33 These amendments include the following:
• Clarifications that applicants must specify how they will integrate information to
account for individuals with behavioral needs both before and following a public
health emergency.
• Clarifications that eligible entities must specify how they will coordinate with
state education, child care, and other relevant agencies.
• The addition of a requirement that applicants must describe how they will
provide technical assistance to certain facilities, such as residential care facilities
and group homes, where there is an increased risk of infectious disease outbreaks
in a PHE.
• A requirement that applicants must issue assurances that relevant staff will
complete preparedness and response trainings as specified.
Section 2112: Supporting access to mental health and substance use disorder
services during public health emergencies
Background
The Substance Abuse and Mental Health Services Administration (SAMHSA) is the federal
agency primarily responsible for supporting community-based mental health and substance use
treatment and prevention services. SAMHSA does not directly deliver treatment services. Rather,
it supports state and local efforts in providing mental health and substance use (collectively
known as behavioral health) services, primarily through funding and technical assistance.
SAMHSA derives most of its statutory authority from Title V of the Public Health Service Act
(PHSA). More specifically, PHSA Section 50134 provides the enumerated authorities of the
Assistant Secretary for Mental Health and Substance Use (Assistant Secretary). Prior to the
PREVENT Pandemics Act, SAMHSA’s general authorities did not include any explicit
responsibilities related to public health emergencies.
Provision

30 Funded territories include American Samoa, Puerto Rico, U.S. Virgin Islands, Guam, and the Northern Marianas.
Funded freely associated states include Micronesia, Palau, and Marshall Islands. For the purposes of this cooperative
agreement, the District of Columbia and the Commonwealth of Puerto Rico receive funding allocations as per states.
Territories, and the nation’s three most populous cities, receive funding allocations per different formulas. 42 U.S.C.
§247d–3a.
31 CDC, “Public Health Emergency Preparedness Program and Guidance,” https://www.cdc.gov/orr/readin.ess/phep/
index.htm.
32 42 U.S.C. §247d–3a(b)(2)
33 42 U.S.C. §247d-3a(b)(2).
34 42 U.S.C. §290aa.
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Section 2112 amends PHSA Section 501 to add an explicit SAMHSA authority to support
continued access to behavioral health services during a public health emergency. The provision
requires SAMHSA to specify a strategy for supporting behavioral health services during or in
response to a public health emergency in SAMHSA’s quadrennial strategic plan, and to provide a
description of such activities in its biennial report to Congress.
In addition, Section 2112 requires the Assistant Secretary of SAMHSA to issue a report to
specified congressional committees reflecting recommendations from SAMHSA’s internal
advisory councils on how to improve behavioral health services during a public health
emergency. The provision also requires GAO to submit to specified congressional committees a
report on SAMHSA programs and activities supporting behavioral health services during the
COVID-19 pandemic, due not later than December 30, 2025. This GAO report is to (1) examine
the role of SAMHSA’s internal advisory councils in supporting SAMHSA’s public health
emergency-related activities, (2) describe how SAMHSA grant awardees altered delivery of
behavioral health services during the COVID-19 PHE and any barriers faced in delivering care,
and (3) describe SAMHSA activities supporting the response to the COVID-19 PHE, including
flexibilities provided to grant awardees or barriers faced in implementing activities.
Section 2113: Trauma care reauthorization
Background
The Patient Protection and Affordable Care Act (ACA, P.L. 111-148) amended and reauthorized a
number of trauma care programs authorized in PHSA Title XII. These provisions were intended
to address a number of recommendations that the Institute of Medicine (now National Academy
of Medicine) made to improve the U.S. emergency and trauma care system.35 These included
designating ASPR as the lead within HHS for emergency and trauma care, authorizing grants to
create regionalized systems for trauma care, allocating additional funds to facilities with large
uncompensated care burdens, and improving the emergency care workforce, among other
provisions. The programs were transferred to the ASPR in the ACA; however, these grant
programs have not been funded since the transfer and modifications made in the ACA.
Provision
Section 2113 makes a number of modifications to PHSA Title XII. Specifically, the provision
• adds new language and a new purpose to the grants authorized in PHSA Section
1201—general grants related to improving trauma care—to add that grants can
be made to states and consortia of states to improve emergency services and
trauma care during a PHE;36
• amends PHSA Section 1202 to replace a rural trauma care grant with new
language creating a program for trauma care in rural areas similar to the prior
program, except that the new program requires the Secretary to award grants,
adds language regarding trauma care (prior language authorized grants for
emergency medical services), specifies eligible entities and granting priority, and
requires grantees to submit reports to the HHS Secretary;37

35 Institute of Medicine, Emergency Medical Services at the Crossroads (Washington, DC: The National Academies
Press, 2006); Institute of Medicine, Hospital-Based Emergency Care At the Breaking Point (Washington, DC: The
National Academies Press, 2006); and Institute of Medicine, Emergency Care for Children: Growing Pains
(Washington, DC: The National Academies Press, 2006).
36 42 U.S.C. §300dd.
37 42 U.S.C. §300d-3.
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• amends PHSA Section 1204 regarding competitive grants for regionalized trauma
systems to rename the section “Competitive Grants for Trauma Centers” and
modify language in the general purposes of the grant and grant activities to (1)
amend the eligible entities for the grant program to include consortia of trauma
centers; (2) add new language about disseminating best practices, facilitating
activities to conduct clinical research; (3) require matching funds as of October 1,
2025; and (4) require a report to be disseminated to certain specified
congressional committees;38 and
• amends PHSA Section 1232 to reauthorize funding from FY2023 through
FY2027.39
Section 2114: Assessment of containment and mitigation of infectious diseases
Background
In response to COVID-19, various jurisdictions executed public health emergency and medical
preparedness and response plans. Although the plans may have shared unique elements, some
jurisdictions used different infection control measures, such as recommendations for isolation and
quarantine.40
Provision
This provision directs GAO to conduct a study and deliver a report to Congress on the emergency
preparedness and response plans of select states and territories that, in response to the COVID-19
pandemic, implemented preparedness and response plans that included isolation and quarantine
recommendations or requirements. This study, due within 18 months of enactment of the
PREVENT Pandemics Act, is to include a review of these plans, an assessment of the extent to
which they facilitated or hindered state and territorial responses, and a description of the technical
assistance provided by the federal government to help states and territories facilitate their
response activities.
Section 2115: Consideration of unique challenges in noncontiguous States and
territories
Background
Noncontiguous states and territories are those that are not connected by land or do not share a
border with other states or territories.41 These jurisdictions can face unique challenges during
public health emergencies. CDC’s Office of Island Affairs, which serves the territories and freely
associated states, asserts that “public health issues affect these islands harder than most places
because of their geographic location and limited local capacity. The remoteness, climate change

38 42 U.S.C. §300d–5.
39 42 U.S.C. §300d–32.
40 Rebecca Katz, Andrea Vaught, Adrienne Formentos, et al., “Raising the Yellow Flag: State Variation in Quarantine
Laws,” Journal of Public Health Management & Practice, vol. 24, no. 4 (July 1, 2019).
41 Cornell Law School: Legal Information Institute, “noncontinguous,” Wex Legal Dictionary,
https://www.law.cornell.edu/wex. Noncontiguous states and territories include Alaska, Hawaii, the five U.S. territories
(American Samoa, Commonwealth of the Northern Mariana Islands, Guam, Puerto Rico, and the U.S. Virgin Islands),
and three freely associated states (Federated States of Micronesia, Republic of Palau, and the Republic of the Marshall
Island).
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vulnerabilities, and limited resources available heighten the public health challenges experienced
in the [territories and freely associated states].”42
Provision
This provision directs the HHS Secretary to conduct quarterly meetings, as appropriate, during
any declared PHEs with noncontiguous states and territories regarding unique public health
challenges associated with the PHE in such areas.
Subtitle B—Improving Public Health Preparedness
and Response Capacity
Chapter 1—Improving Public Health Emergency Responses
Section 2201: Addressing factors related to improving health outcomes
Background
The PHSA currently includes many authorizations used for public health and health promotion
programs designed to address health disparities. For example, PHSA Section 317 is a general and
permanent authorization for preventive health services programs.43 This authorization is used as a
basis for many CDC public health programs, including, for example, programs to promote
evidence-based strategies to improve nutrition and physical activity,44 as well as to reduce health
disparities among racial and ethnic populations with the highest burden of chronic disease.45
During the COVID-19 pandemic, Congress provided relief funding designed to directly address
health disparities exacerbated by the pandemic.46
Provision
Section 2201 adds a new PHSA Section 317V, which authorizes two programs for improving
health outcomes. The first program allows the HHS Secretary to award funding for evidence-
based projects to improve health outcomes. Eligible funding recipients include SLTT health
departments, other public and private entities, and partnerships or consortia among organizations.
Applicants must demonstrate a history of working with established community-based
organizations to address health outcomes (if not already a community-based organization), and
applicants must submit a plan based on a community needs assessment. Award recipients are to
use funds for at least one of the following: (1) to support the implementation, evaluation, and
dissemination of strategies to address factors related to health outcomes; (2) to establish,
maintain, or improve technology platforms or networks to support coordination, information

42 CDC, “Office of Island Affairs – Fact Sheet,” https://www.cdc.gov/islandaffairs/factsheet.html. CDC’s Office of
Island Affairs helps connect the territories and freely associated states to CDC funding and resources.
43 42 U.S.C. §247b.
44 CDC, “The State Physical Activity and Nutrition Program (SPAN),” CDC-RFA-DP-23-0012, March 28, 2023, p. 4,
https://www.grants.gov/web/grants/view-opportunity.html?oppId=342954.
45 CDC, Racial and Ethnic Approaches to Community Health (REACH), CDC-RFA-DP-23-0014, April 11, 2023, p. 4,
https://www.grants.gov/web/grants/view-opportunity.html?oppId=342940.
46 For example, not less than $2.5 billion of a $22.4 billion testing and contact tracing appropriation was for testing and
contact tracing strategies among “high-risk and underserved populations, including racial and ethnic minority
populations and rural communities” in the Public Health and Social Services Emergency Fund account in P.L. 116-260,
Division M.
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sharing, and technical assistance among entities; (3) to implement best practices for improving
health outcomes and reducing disease among underserved populations; and (4) to support
consideration of factors related to health outcomes in preparing for and responding to public
health emergencies through outreach, education, research, and other relevant activities.
For the second program, the HHS Secretary may award funding to minority-serving institutions
(as defined in the Higher Education Act of 1965), in consultation with the Office of Minority
Health, ONC, and the Administrator of the Administration for Community Living. Awardees are
to (1) identify or facilitate the development of best practices to support improved health outcomes
for underserved populations; (2) provide technical assistance, training, and evaluation assistance
to award recipients receiving funding for evidence-based projects to improve health outcomes
(described in the paragraph above); (3) disseminate best practices; and (4) leverage, establish, or
operate regional centers to develop, evaluate, and disseminate effective strategies on factors
related to health outcomes, including supporting research and training related to such strategies.
For both programs authorized under the new PHSA Section 317V, funding may be awarded for a
period up to five years and may be extended for an additional period up to three years. The
Secretary is to submit a report on funded activities and related outcomes to specified
congressional committees no later than September 30, 2026.
PHSA Section 317V authorizes an appropriation of $35 million for each of FY2023 through
FY2027. Of the amount for each fiscal year, 5% is reserved for tribal organizations, as specified.
Within four years of enactment, GAO is to report to specified congressional committees on the
program authorized under PHSA Section 317V, including a review of the outcomes and
effectiveness of the program and coordination with other HHS programs with similar goals to
ensure that there was no unnecessary duplication of efforts.
Chapter 2—Improving State, Local, and Tribal Public Health Data
Background for Sections 2211-2216
The COVID-19 pandemic exposed the challenges associated with collecting and reporting
national health data on a rapidly changing pandemic in the context of the U.S. federal public
health system—where many of the laws and programs for public health data are based at the
SLTT level.47 In addition, the pandemic demonstrated some of the potential for modernized
approaches to public health surveillance and data analysis, such as through surveillance using
genome sequencing or by using newer modeling and forecasting methods to predict the trajectory
of outbreaks.48
Previously, through the Pandemic and All-Hazards Preparedness Act of 2006 (P.L. 109-417) and
subsequent reauthorizations before the COVID-19 pandemic,49 Congress has directed HHS in
PHSA Section 319D to
establish near real-time electronic nationwide public health situational awareness
capability through an interoperable network of systems to share data and information to
enhance early detection of rapid response to, and management of, potentially catastrophic

47 CRS Report R46588, Tracking COVID-19: U.S. Public Health Surveillance and Data.
48 CRS In Focus IF11789, COVID-19 Variants: Vaccines, Diagnostics, and Therapeutics, and U.S. Government
Accountability Office, Science & Tech Spotlight: COVID-19 Modeling, GAO-20-582SP, June 4, 2020,
https://www.gao.gov/products/gao-20-582sp.
49 Pandemic and All-Hazards Preparedness Reauthorization Act of 2013 (P.L. 113-5) and the Pandemic and All-
Hazards Preparedness and Advancing Innovation Act of 2019 (P.L. 116-22).
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infectious disease outbreaks and other public health emergencies that originate
domestically or abroad.
GAO reported that, as of March 2022, HHS had not yet established this capability or taken all
statutorily required steps to plan for such a capability. The HHS Secretary had designated the
Assistant Secretary for Preparedness and Response as responsible for developing the strategy.50
CDC is the primary HHS agency that directly receives and analyzes public health surveillance
data related to infectious diseases. CDC generally receives de-identified public health
surveillance data—including on cases, testing, deaths, and hospitalizations—from all or a subset
of U.S. jurisdictions based on data sharing agreements with those jurisdictions.51 U.S.
jurisdictions have differing legal requirements and systems for collecting different types of public
health data.52 Jurisdictions also generally rely on diverse health care entities—such as
laboratories, hospitals, and outpatient health care facilities—to share data and meet reporting
requirements. In the past, data sharing among entities has sometimes relied on outdated means of
exchange, such as by fax machines or Excel spreadsheets. CDC has funded public health
surveillance systems at the SLTT level and has encouraged jurisdictions to follow recommended
standards for data collection.53 Despite this funding and the recommended standards, SLTT
jurisdictions collected public health data in different ways during and before the pandemic, which
affected the timeliness and adequacy of data for response.54
During the pandemic, Congress and the executive branch implemented federal-level public health
data reporting requirements, including a laboratory test result reporting requirement in the
CARES Act (P.L. 116-136; Section 18115) and hospital and nursing home requirements through
CMS regulations.55
Throughout the pandemic, Congress provided supplemental appropriations through six different
COVID-19 relief laws that included funding for public health surveillance and data systems.56 For
example, much of the more than $59 billion in COVID-19 grants that CDC has awarded to SLTT
jurisdictions from these laws can be used, in part, for surveillance and data-related activities.57
The American Rescue Plan Act of 2021 (ARPA; P.L. 117-2) provided specific funding to establish

50 GAO, COVID-19: Pandemic Lessons Highlight Need for Public Health Situational Awareness Network, GAO-22-
104600, June 2022, https://www.gao.gov/assets/730/721426.pdf.
51 CRS Report R46588, Tracking COVID-19: U.S. Public Health Surveillance and Data, and CDC, “Where Does our
Data Come From?,” https://www.cdc.gov/surveillance/data-modernization/basics/
where_does_our_data_come_from.html.
52 Association of State and Territorial Health Officials, Legal Landscape of Public Health Data: A Scan of State Laws
Governing Public Health Data, March 2023, https://www.astho.org/globalassets/report/legal-landscape-of-ph-data-
scan-of-state-laws.pdf, and Macarena C. Garcia, Nedra Y. Garrett, Vivian Singletary, et al., “An Assessment of
Information Exchange Practices, Challenges and Opportunities to Support U.S. Disease Surveillance in Three States,”
Journal of Public Health Management and Practice, vol. 24, no. 6 (2018), pp. 546-553.
53 U.S. Government Accountability Office, COVID-19: Current and Future Federal Preparedness Requires Fixes to
Improve Health Data and Address Improper Payments, GAO-22-105397, April 27, 2022, pp. 49-54,
https://www.gao.gov/products/gao-22-105397, and CRS Report R46588, Tracking COVID-19: U.S. Public Health
Surveillance and Data.
54 CDC, “Where Does our Data Come From?,” https://www.cdc.gov/surveillance/data-modernization/basics/
where_does_our_data_come_from.html.
55 42 C.F.R. §482.42(e), 42 C.F.R. §485.640(d), and 42 C.F.R. §483.80(g)
56 CRS Report R46711, U.S. Public Health Service: COVID-19 Supplemental Appropriations in the 116th Congress,
and CRS Report R46834, American Rescue Plan Act of 2021 (P.L. 117-2): Public Health, Medical Supply Chain,
Health Services, and Related Provisions.
57 CDC, “CDC COVID-19 State, Tribal, Local and Territorial Funding,” https://www.cdc.gov/budget/fact-sheets/covid-
19/funding/index.html. Allowable uses of funds vary by grant, see links at the end of the website.
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a Center for Forecasting and Outbreak Analytics at CDC (Section 2404), as well as for genomic
sequencing and surveillance (Section 2402). CDC established the Center for Forecasting and
Outbreak Analytics in April 2022 using $200 million of the ARPA funds.58 In addition, the Biden
Administration announced that the $1.75 billion genomic surveillance appropriation would be
used as follows: $1 billion for CDC and SLTT jurisdictions to expand sequencing capacity, $400
million for new Centers of Excellence in Genomic Epidemiology that operate as partnerships
between state public health agencies and academic institutions, and $300 million to build a
National Bioinformatics Infrastructure.59
CDC has received a total of $1.38 billion to date for its Data Modernization Initiative (DMI) from
both regular and COVID-19 supplemental appropriations.60 CDC’s DMI is an effort to modernize
the way public health data are collected, shared, and analyzed in the United States to enable rapid
and comprehensive data on health threats.61 As a part of the DMI, CDC has partnered with the
Office of the National Coordinator for Health Information Technology (ONC) to establish new
standards and regulations for facilitating the modernization of data exchange between the health
care and public health sectors, with feedback gathered from federal advisory committees.62 In
addition, Congress required CDC data modernization activities and authorized a related grant
program as a part of the Consolidated Appropriations Act, 2021 (P.L. 116-260; Division BB,
Section 314), which enacted PHSA Section 2823.
Section 2211: Modernizing State, local, and tribal biosurveillance capabilities
and infectious disease data
Provision
Section 2211 amends PHSA Section 319D, which addresses CDC and other HHS biosurveillance
and public health emergency response capabilities.63 The provision makes several amendments to
clarify CDC’s required capacities for responding to bioterrorism and other public health threats
(in subsection a). These capacities include training personnel, improving communications
facilities and networks, improving capabilities for public health surveillance and reporting, and
improving laboratory facilities. Under prior law, such activities were allowed but not required.
In addition, Section 2211 makes several amendments to the existing authorizations for HHS to
establish an integrated system of public health alert communications and surveillance networks
(in subsection b), to establish a near real-time electronic nationwide public health situational
awareness capability through an interoperable network of systems (in subsection c), and to
implement a state or regional grant program for situational awareness systems (in subsection d).
In particular, Section 2211 makes several amendments to address the privacy of information

58 CDC, “CDC Launches New Center for Forecasting and Outbreak Analytics,” April 2022, https://www.cdc.gov/
media/releases/2022/p0419-forecasting-center.html.
59 The White House, “Fact Sheet: Biden Administration Announces $1.7 Billion Investment to Fight COVID-⁠19
Variants,” press release, April 16, 2021, https://www.whitehouse.gov/briefing-room/statements-releases/2021/04/16/
fact-sheet-biden-administration-announces-1-7-billion-investment-to-fight-covid-19-variants/.
60 CDC, “Notable DMI Milestones: 2019-2023,” https://www.cdc.gov/surveillance/data-modernization/milestones.html
and CRS analysis of appropriations.
61 CDC “Data Modernization Initiative (DMI): The Basics,” https://www.cdc.gov/surveillance/data-modernization/
basics/index.html.
62 CDC, “Advancing Interoperability for Public Health,” https://www.cdc.gov/surveillance/policy-standards/
interoperability.html, and ONC, “Public Health Data Systems Task Force 2022,” https://www.healthit.gov/hitac/
committees/public-health-data-systems-task-force-2022.
63 42 U.S.C. §247d-4.
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collected in such systems, including by adding requirements throughout PHSA Section 319D that
information is collected in a manner that protects privacy and security as required by applicable
federal and state law. Section 2211 makes many other amendments, including those related to
incorporating tribal data systems into the networks, ensuring data quality, improving laboratory
data reporting, improving data exchange, ensuring consultation with state officials, and ensuring
that standards align with those in PHSA Section 2823, the CDC data modernization authorization.
Section 2211 requires the Secretary to convene a public meeting for providing input on the
network (subsection c) within 180 days of enactment. It also requires the Secretary to update a
strategy and implementation plan for the network every five years. Among other things, the
strategy implementation plan is to implement applicable lessons learned from recent public health
emergencies. In addition, the plan must identify and demonstrate measurable steps to further
develop and integrate infectious disease detection, to support laboratory test result sharing, and to
improve coordination among SLTT public health officials, clinical laboratories, and others with
expertise in public health surveillance.
Nothing in the amended PHSA Section 319D(c) may be construed to (1) supplant relevant SLTT
activities related to public health surveillance, or (2) alter the Secretary’s data collection authority
with respect to types of data. The Secretary is required to ensure that activities under the state
grant program do not duplicate efforts of other HHS agencies.
Section 2211 amends PHSA Section 319D to authorize appropriations of $25 million for each of
FY2022 and FY2023 for CDC’s facilities and capacities (subsection a), and $136 million for each
of FY2022 and FY2023 for the interoperable networks and public health situational awareness
capabilities (in subsections b, c, and d).
Section 2212: Genomic sequencing, analytics, and public health surveillance of
pathogens
Provision
Section 2212 includes two main provisions related to genomic sequencing and surveillance. First,
the provision directs the HHS Secretary to issue guidance related to genomic sequencing of
pathogens (subsection a). The guidance is to support collaboration among federal agencies related
to genomic sequencing of pathogens, including the use of new and innovative approaches, to
improve public health surveillance and response activities. The guidance is also to address secure
sharing of sequence data and to ensure privacy protection consistent with state and federal law.
Second, Section 2212 formally authorizes a genomic sequencing, analytics, and surveillance
program at CDC by adding a new PHSA Section 2824 (subsection b). The new PHSA Section
2824 requires CDC to strengthen and expand activities related to genomic sequencing of
pathogens in consultation with NIH and other departments and agencies. CDC is to address
technological and workforce capabilities for genomic sequencing, and to provide technical
assistance to SLTT public health agencies, including those receiving Epidemiology and
Laboratory Capacity grants. The section authorizes CDC to award funding to entities with
expertise in genomic sequencing for public health purposes, including academic laboratories, for
achieving these goals. PHSA Section 2824 also authorizes funding awards to public health
agencies to establish centers of excellence to promote innovation in pathogen genomics and
molecular epidemiology. These centers are to develop new surveillance and epidemiology
approaches, along with assisting in responses and developing training materials for other experts.
To receive an award, public health agencies must partner with academic institutions with relevant
expertise. This section does not authorize an appropriation.
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Under Section 2212, CDC must report to specified congressional committees within 90 days after
enactment and 90 days after expenditure of all funds outlining how funds under American Rescue
Plan Act of 2021 (ARPA; P.L. 117-2) Section 2402 were expended as of that date. ARPA Section
2402 appropriated funding for genomic sequencing and surveillance.
Section 2213: Supporting State, local, and tribal public health data
Provision
Section 2213 is a multicomponent authorization that addresses several aspects of public health
data policy. First, Section 2213 amends requirements under PHSA Section 2823(a)(2),64 which
authorizes the HHS Secretary to establish standards for CDC public health data systems and
SLTT governments receiving grant funding under that section. The amendment adds specificity to
the existing law by requiring the Secretary to develop such standards no later than two years after
enactment. The amended PHSA Section 2823 further stipulates that, to eliminate duplicative
efforts when creating these standards, the Secretary, in conjunction with the ONC, may draw
upon input gathered (including from an existing advisory committee) and materials created prior
to enactment. These standards must comply with existing federal laws pertaining to standards and
implementation specifications for health information and technology. None of the amendments to
PHSA Section 2823 may be construed to preempt relevant federal or state information privacy or
security law.
Second, Section 2213 requires that, within one year of enactment, ONC conduct a study to review
the use of standards for electronic ordering and reporting of laboratory test results. The study
must focus on (1) the extent of laboratory standard use, (2) compliance and effects on
interoperability, and (3) challenges to collection of demographic data and compliance with
standards, among other things. Within two years of enactment, ONC must submit a report, based
on this study, to select congressional committees, as specified.
Third, under Section 2213, the Secretary is required to facilitate the development of and updates
to HHS interagency data use agreements between CDC, ASPR, other relevant agencies and
offices within HHS, and other federal agencies to prepare for and respond to potential or declared
public health emergencies. In carrying out this requirement, the Secretary must adhere to specific
further requirements, including, for example, addressing methods of granting access to other
agencies, considering minimum necessary principles of data sharing for appropriate use, and
using privacy and security protections. The Secretary is further allowed to update data-related
agreements and contracts between CDC, ASPR, and external entities, including, for example,
SLTT health departments, laboratories, and health care providers, in order to prepare for and
respond to public health emergencies. Within 90 days of enactment, the Secretary shall report to
select congressional committees on the status of agreements among stakeholders both internal and
external to HHS.
Fourth, Section 2213 amends part A of PHSA Title III to add a new PHSA Section 310B,
“Improving State, Local, and Tribal Information Sharing.” The new section allows the Secretary
to conduct activities to improve the availability of relevant public health data on communicable
disease and to facilitate information sharing between CDC, ASPR, and SLTT public health
officials, in consultation with nonfederal public health officials. Such public health data can
include data from health care facilities, laboratories, health information exchanges, and SLTT
health departments. When possible, the Secretary shall ensure that the data disclosed are the
minimum necessary for public health purposes. The Secretary shall consult with public health

64 42 U.S.C. §300hh–33.
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officials and relevant stakeholders to determine the most effective content, form, and manner for
data sharing, consistent with existing federal law, to enable nonfederal health department
communicable disease response, including the collection and reporting of demographic and other
relevant data elements. Data gathered may be exempt from disclosure under FOIA (5 U.S.C.
§552) if it identifies an individual or if there is even a small risk it could identify, alone or in
combination with other available resources, an individual.
Fifth, Section 2213 additionally requires the Secretary to award funding for identifying,
developing, or disseminating best practices in electronic health information and the use of
designated standards and implementation specifications to improve the quality and completeness
of public health data, including demographic data. Eligible entities for the program include SLTT
governments, health care providers, academic medical centers, community-based organizations,
other tribal organizations, and other appropriate public or private nonprofit entities. Award-
receiving entities shall develop and test health care provider training best practices with regard to
activities surrounding the use of standards and implementation specifications that assist in the
capture, access, exchange, and use of electronic health information. Such electronic health
information can include demographic information, disability status, veteran status, and functional
status. These endeavors must include, at a minimum, those related to (1) using and improving
data standards and implementation specifications, (2) improving communications with culturally
diverse patients to better capture their demographic information, (3) developing methods for
accurately recording patient responses, (4) educating providers on the importance of accurate data
collection and recording and the utility of the data, and (5) providing information regarding how
data will be de-identified if used for public health purposes, as applicable. Award recipients shall
submit a report to the Secretary of best practices developed. The Secretary, within one year of the
program’s completion, shall submit a report to Congress regarding the success of identified best
practices and recommendations for improving public health and reducing disparities through
improving the capture, access, exchange, and use of data. The Secretary shall ensure funded
activities and programs are not unnecessarily duplicative. There is no authorization of
appropriations for this program.
Finally, nothing in Section 2213 may be construed to (1) supplant relevant SLTT activities related
to public health surveillance, (2) alter the Secretary’s data collection authority with respect to
types of data, or (3) modify relevant federal and state information privacy or security law.
Section 2214: Epidemic forecasting and outbreak analytics
Provision
Section 2214 adds a new PHSA Section 2825, which formally authorizes epidemic forecasting
and analytics activities at CDC to enhance the prediction, modeling and forecasting of potential
public health emergencies and other infectious disease outbreaks. The Secretary is to identify
strategies to leverage the capabilities of other public and private entities in these efforts, including
through collaborative partnerships. CDC may consider public health and other data sources
related to public health emergencies and other infectious disease outbreaks in these efforts.
CDC is to report to specified congressional committees on the progress of activities within one
year of enactment and then annually for the subsequent four years.
Section 2215: Public health data transparency
Provision
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Section 2215 requires the HHS Secretary to issue a report within one year of enactment assessing
CDC’s collection and dissemination of public health data related to a public health emergency
declared under PHSA Section 319 or a potential public health emergency. The report is to assess
practices, objectives, and associated progress and challenges in achieving such objectives.
No later than 180 days after submitting the report, CDC is to submit a plan to specified
congressional committees that includes (1) steps to improve the timely reporting and
dissemination of de-identified public health data related to a public health emergency and
associated barriers, (2) recommendations to Congress regarding gaps in practices and objectives,
and (3) considerations regarding the requirements and limitations of data use agreements for such
purposes, and any efforts undertaken to address those requirements and limitations.
Section 2216: GAO report on public health preparedness, response, and
recovery data capabilities
Provision
Section 2216 directs GAO to conduct a study on HHS’ efforts to ensure that data capabilities
related to public health preparedness, response, and recovery for pandemic and other biological
threats are not unnecessarily duplicative, overlapping, or fragmented. The study is to include (1) a
comprehensive list of all relevant data collection efforts as identified by the department; (2) an
analysis of duplication, overlap, or fragmentation in such programs; (3) documentation of HHS
efforts to reduce duplication, improve coordination, and associated challenges; (4) reporting of
any practices that threaten individual privacy and recommendations to improve privacy of
individual, identifiable data; and (5) a description of the funding dedicated to each data collection
program.
GAO must provide a briefing no later than six months after enactment and a complete report no
later than 18 months after enactment to specified congressional committees. The report is to
include recommendations for related data programs to (1) streamline data collection and reduce
fragmentation and any associated challenges, (2) reduce duplication in such programs, and (3)
improve information sharing across programs.
Chapter 3—Revitalizing the Public Health Workforce
COVID-19 pandemic preparedness and response have required mobilization of the public health
workforce and the patient care workforce to test, treat, and vaccinate patients and to engage in
outbreak control efforts. For both workforces, the pandemic revealed underlying challenges
related to workforce shortages overall, in certain disciplines, and in specific geographic locations.
In addition, the pandemic may have exacerbated issues related to clinician burnout. One survey
found that 52% of providers reported experiencing burnout and 62% reported that worry or stress
during the pandemic had adversely affected their mental health.65 The American Rescue Plan Act
(P.L. 117-2) included additional funding for several new and existing health workforce programs.

65 Scott Clement, Cece Pascual, and Monica Ulamanu, “Stress on the Front Lines of Covid-19: Health Care Workers
Share the Hardest Part of Working During the Pandemic,” Washington Post, April 6, 2021,
https://www.washingtonpost.com/health/2021/04/06/stress-front-lines-health-care-workers-share-hardest-parts-
working-during-pandemic/. Other studies have shown increased anxiety, depression, sleep problems, and distress
among health care workers during the COVID-19 pandemic. See, for example, Ashley E. Muller, Elisabet V. Hafstad,
Jan P. W. Himmels, et al., “The Mental Health Impact of the COVID-19 Pandemic on Healthcare Workers, and
Interventions to Help Them: A Rapid Systematic Review,” Psychiatry Research, vol. 293 (November 2020).
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Section 2221: Improving recruitment and retention of the frontline public
health workforce
Background
PHSA Section 776 authorized the Public Health Workforce Loan Repayment Program, a loan
repayment program to support public health professionals at federal state, local, and tribal public
health agencies.66 Individuals were eligible for loan repayment if they are in their final year of
study for a degree in public health or a health profession and have accepted employment (or a
related training fellowship) at an eligible public health agency. Individuals were also eligible if
they have completed training during the preceding 10-year period. Eligible individuals had to be
U.S. citizens, may not have had another service obligation, and must apply, and enter into a
contract with the HHS Secretary. The section also specified the penalties for breach of contract. It
specified that participants will receive $35,000 in loan repayment for each year served, with a
maximum total loan repayment award of $105,000. The Secretary was allowed to provide
additional payments for an individual’s tax liability. Authorizations of appropriations for this
program were from FY2010 through FY2015; this program has not been funded in recent years.
No loan repayments have been made under this program in recent years.
There are also separate federal loan repayment programs for public health professionals, such as
the CDC Educational Loan Repayment Program for Health Professionals, for CDC staff who
have participated in selected CDC fellowship programs as authorized by PHSA Section 317F.67
Provision
The provision amends PHSA Section 776 to make a number of changes to the loan repayment
program. Notably, it removes eligibility for individuals at federal agencies; instead, the program
is to recruit and retain individuals at state, local, and tribal public health agencies. The provision
makes a number of technical changes to the loan repayment program, for example, to make
graduates (or soon to be graduates) of additional degree programs eligible for loan repayment,
including those with certificates and those with training in specified data science fields. It also
requires a service commitment of at least three consecutive years; increases the annual loan
repayment amount to $50,000 per year and the maximum loan repayment amount to $150,000
total; and adds requirements that the Secretary, when making awards, attempt to achieve a
balance in geographical regions, urban and rural participation, and participation by employees at
state, local, and tribal health departments. The provision also adds language that specifies eligible
loan types and adds that the Secretary may waive or suspend penalties for individuals who fail to
complete their service commitment.
The provision also establishes a pilot program known as the Bio-Preparedness Workforce Pilot
Program to provide loan repayment for health professionals who have expertise in infectious
disease and emergency preparedness and response activities as a part of PHSA Section 776. The
pilot will be administered in the same way as the Public Health Loan Repayment program in
PHSA Section 776, except that it would permit individuals to fulfill their service commitment in
federal health care facilities, in nonprofit health care facilities located in health professional
shortage areas, in entities funded by the Ryan White HIV/AIDS program or the Indian Health
Service, or at any other entity determined appropriate by the Secretary. The provision requires
that the new program not duplicate the efforts of other federal loan repayment programs,

66 42 U.S.C. §295f–1.
67 CDC, “Educational Loan Repayment Program for Health Professionals,” https://www.cdc.gov/fellowships/
loanrepayment.html.
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including the National Health Service Corps, and be evaluated with a report to Congress that
includes recommendations on whether the program should be extended.
Finally, the provision authorizes an appropriation of $100 million for each of FY2023 through
FY2025, and requires a GAO study on the health care workforce that includes certain specified
elements. This study would be completed no later than two years after enactment and is to be
submitted to specified congressional committees.
Section 2222: Awards to support community health workers and
community health
Background
PHSA Section 399V authorized CDC to award grants for using community health workers to
promote positive health behaviors and outcomes for populations in medically underserved
communities.68 Community health workers funded through the program were to provide
education and outreach related to health problems, health behaviors, health care program
enrollment, and other health care services access. CRS has not identified a dedicated CDC
community health worker grant program carried out using authority in PHSA 399V.69 During the
COVID-19 Pandemic, CDC funded a Community Health Workers for COVID Response and
Resilient Communities (CCR) initiative using COVID-19 relief funds.70 In addition, HRSA made
awards to support 83 community health worker training program grantees using funding from
ARPA.71
Provision
This provision amends PHSA Section 399V to replace the overall statutory purpose of the
community health worker grant program. The amended section requires the Secretary to award
grants, contracts, or cooperative agreements to eligible entities to support community health
worker programs that target improving health behaviors in medically underserved communities,
including by addressing ongoing and longer-term community health needs, and by building the
capacity of the community health worker workforce. The provision amends PHSA Section 399V
to add language to the existing community health worker program that makes grants, contracts, or
cooperative agreements awarded subject to state laws or requirements regarding scope of
licensure, registration, or certification for community health workers. The provision also makes
technical corrections to PHSA Section 399V and adds language for grant purposes that include
that the funds should be used to (1) recruit, hire, train, and retain community health workers that
meet the needs of the community, and (2) focus on health conditions that are prevalent in the
medically underserved community or in a community that would require additional support under
a public health emergency. The provision also adds language regarding promoting health
behaviors, reducing health disparities, and serving rural populations. The provision adds new
subsections to PHSA Section 399V that authorize the Secretary to provide technical assistance to
awardees, require the Secretary to disseminate best practices regarding the recruitment and
retention of community health workers, and require a report to Congress about the effectiveness

68 42 U.S.C. §280g–11.
69 CDC has cited PHSA Section 399V as authorizing legislation for is Public Health Scientific Services budget activity;
however, it is unclear what programs or activities are carried out using this authority.
70 CDC, “Community Health Workers for COVID Response and Resilient Communities (CCR),” https://www.cdc.gov/
covid-community-health-workers/index.html.
71 HHS, “With New American Rescue Plan Funding, HHS Expands and Strengthens the Community and Public Health
Workforce,” press release, September 30, 2022, https://www.hhs.gov/about/news/2022/09/30/new-american-rescue-
plan-funding-hhs-expands-and-strengthens-community-and-public-health-workforce.html.
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of the program. Finally, the provision amends the section’s authorization of appropriations to
authorize $50 million for each of FY2023 through FY2027, defines a number of terms, and
requires a GAO study that examines the duplication between training programs administered by
HRSA.
Section 2223: Improving public health emergency response capacity
Background
The authority to directly hire individuals can allow federal agencies to quickly fill vacancies
when a critical hiring need or severe candidate shortage exists.72 HHS and other stakeholders
have asserted that the use of such an authority during a public health emergency would allow
HHS to respond to an incident in a more rapid manner.73
Provision
This provision amends PHSA Section 319 to add a new subsection that authorizes the HHS
Secretary to directly appoint a limited number of individuals to positions in HHS to support an
initial response to a declared public health emergency.74 The HHS Secretary can make up to 400
appointments for critical hiring needs and up to 100 appointments for severe shortage of
candidates per each fiscal year in which the HHS Secretary makes a PHE declaration (not
including renewals). The Secretary must maintain records of the appointments and, under
specified conditions, provide notices to Congress on the use of this authority, as well as provide
annual reports to Congress. One year after the initial report, GAO shall submit a report to
Congress on the use of this authority. The appointment authority is scheduled to expire on
September 30, 2028.
Section 2224: Increasing educational opportunities for allied health
professions
Background
PHSA Section 755 authorized grants or contracts to support training in allied health professions
through a number of specified potential grantee activities, including expanding program
enrollment; providing training; establishing community-based training, including in rural and
underserved areas; curriculum development; interdisciplinary training; and providing trainee
financial assistance, amongst other purposes.75 The section did not specify “allied health fields,”
but included language about training to work with geriatric populations and in maternal and child
health, which was added in the CARES Act (P.L. 116-136) in 2020.76 This section has not been
funded in recent years.
Provision
The provision amends PHSA Section 755 to add new language describing the activities the grant
is to support. The provision stipulates that grant funds be used to increase educational

72 U.S. Office of Personnel Management (OPM), “Direct Hire Authority,” https://www.opm.gov/policy-data-oversight/
hiring-information/direct-hire-authority/#url=Fact-Shee
73 Department of Health and Human Services Emergency Fund, Public Health and Social Services FY 2024:
Justification of Estimates for Appropriations Committee , p. 66, https://www.hhs.gov/sites/default/files/fy-2024-phssef-
cj.pdf.
74 42 U.S.C. §247d.
75 42 U.S.C. §294e.
76 CRS Report R46334, Selected Health Provisions in Title III of the CARES Act (P.L. 116-136).
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opportunities in physical therapy, occupational therapy, respiratory therapy, audiology, and speech
language pathology, which may include offering scholarships or stipends, among other activities
that aim to improve retention of individuals from disadvantaged communities in these health
professions.
Section 2225: Public Health Service Corps annual and sick leave
Background
The United States Public Health Service (USPHS) Commission Corps is a uniformed service in
HHS. It is composed of individuals from varying health professions who can augment emergency
and disaster responses. Some members of the Corps serve as full-time federal employees while on
duty (Regular Corps), while others are activated only at particular times (Ready Reserve Corps).77
The amount of annual leave that officers may accumulate while on active duty is specified in
law.78 During the COVID-19 pandemic, many USPHS officers were deployed and unable to take
annual leave. Under prior law, many deployed officers would have lost leave accumulated during
the pandemic, as the amount was capped at 60 days.79
Provision
This provision amends PHSA Section 219 to allow regulations authorizing accumulated annual
leave for commissioned officers of the Regular Corps or Ready Reserves Corps on active duty to
be updated from 60 to 120 days.80
Section 2226: Leadership exchange pilot for public health and medical
preparedness and response positions at the Department of Health and Human
Services
Background
During public health emergency responses, HHS staff often support SLTT health agencies and
work with other federal agencies, such as the Federal Emergency Management Agency (FEMA).
Some have argued that increased practical experience in SLTT agencies or other federal
emergency agencies might help HHS staff provide better service and support during
emergencies.81
Provision
This provision amends PHSA Title XXVIII by adding a new Section 2826, which gives the HHS
Secretary the authority to, not a year later than the enactment of the PREVENT Pandemics Act,
establish a voluntary pilot program to provide additional field training to certain HHS employees
engaged in activities related to public health preparedness and response.82 The program will

77 HHS, Ready Reserve Corps Management, CCI 322.06, June 14, 2021, https://dcp.psc.gov/ccmis/ccis/documents/
CCI_322.06.pdf.
78 PHSA §219; 42 U.S.C. §210-1.
79 See “Letter from Military Coalition to Appropriations Committee Leaders,” September 18, 2020, available at
https://www.moaa.org/content/publications-and-media/news-articles/2020-news-articles/advocacy/leave-policy-
change-is-good-news-for-usphs-commissioned-corps-members/.
80 42 U.S.C. §210-1.
81 See, for example, Center for Strategic and International Studies, Building the CDC the Country Needs, 2023, pp. 21-
22, https://csis-website-prod.s3.amazonaws.com/s3fs-public/publication/230112_Morrison_Building_CDC.pdf?
VersionId=kTKB3urWn1bfZpXuCqixfxzHfT8AUcIM.
82 42 U.S.C. §300hh et seq.
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provide fellowships, details, and other relevant placements with federal agencies, departments, or
state and local health departments for a maximum of two years and shall not exceed five years.
The HHS Secretary shall issue guidance for identifying these opportunities. At the conclusion of
this program, the HHS Secretary shall issue a report to Congress detailing the number of
individuals who participated, a description of their professional growth, and an assessment of the
program, including a recommendation on whether it should be continued.
Section 2227: Continuing educational support for health professionals serving
in rural and underserved communities
Background
PHSA Section 752 required the Secretary to make grants or enter into contracts with eligible
entities for specified activities to improve health care, increase retention and representation of
minority faculty members, enhance practice environments, and disseminate information and
education support to reduce professional isolation.83 The provision specified eligible entities,
required an application, and specified how funds must be used, including to provide distance
education, continuing education, collaborative education, and telelearning activities with priority
for training in primary care. The section authorized an appropriation of $5 million for each of
FY2010 through FY2014 and has not been funded in recent years.
Provision
The provision amends PHSA Section 752 to retitle the program “Continuing Education Support
for Health Professionals Serving in Rural and Underserved Communities.” It amends the program
to require the Secretary to make grants or contracts with eligible entities to support access to
accredited continuing medical education for primary care physicians and health care providers at
community health centers or rural health clinics. In addition to creating new application
requirements, it amends the use of funds to specify that specialty training for primary care
providers be prioritized and that the goal of this training is to improve retention and increase
access to specialty care for community health center and rural health clinic patients. The
provision (1) adds clarifying language stating that funds may be used for training with an in-
person clinical training components, (2) specifies that grantees may not use more than 5% of the
grant funding for administrative expenses, (3) requires that the amended program may not
duplicate other HRSA activities, including those authorized under PHSA Section 330N. (PHSA
Section 330N authorizes a grant program for technology-enabled learning and capacity building
for health care entities in rural, frontier, or health care shortage areas, or that serve Native
American populations, and has been funded under HRSA’s Office of Rural Health as the
Telehealth Technology-Enabled Learning Program). Finally, the provision amends the
authorization of appropriations in PHSA Section 752 to authorize $5 million for each of FY2023
through FY2025.
Chapter 4—Enhancing Public Health Preparedness and Response
Section 2231: Centers for public health preparedness and response
Background

83 42 U.S.C. §294b.
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PHSA Section 319F authorized a program to fund Centers for Public Health Preparedness (the
Centers) at accredited schools of public health.84 These Centers were responsible for establishing
degree program curricula and training programs on essential public health security capabilities
consistent with the National Health Security Strategy. The Centers have been required to conduct
research on public health preparedness and response systems, and to collaborate with SLTT health
departments to assess community preparedness and response needs, evaluate programs and
activities, and develop training and education materials. This program has been administered as
CDC’s Academic Centers for Public Health Preparedness, and has received roughly $8 million to
$9 million per year in recent years.85
Provision
Section 2231 amends PHSA Section 319F to replace the preexisting Centers for Public Health
Preparedness authorization with a new Centers for Public Health Preparedness and Response
program authorization.86 Funded institutes of higher education and other nonprofit entities are
required to coordinate with SLTT public health agencies and health care entities. Funds may be
used to carry out activities to advance public health preparedness and response capabilities,
including (1) identifying, translating, and disseminating research findings or strategies into
evidence-based best practices related to public health preparedness; (2) improving awareness of
such practices among stakeholders and the public; (3) utilizing and expanding technological and
analytical capabilities to inform preparedness and response efforts; (4) participating in drills and
exercises; and (5) providing technical assistance and expertise to SLTT public health agencies and
other appropriate entities. CDC must support at least 10 Centers, subject to the availability of
appropriations, to be distributed geographically throughout the United States.
Section 2231 also strikes Section 319G of the PHSA, which established a demonstration program
to enhance bioterrorism training, coordination, and readiness.87
Section 2232: Vaccine distribution plans
Background
The Pandemic and All-Hazards Preparedness Act (PAHPA, P.L. 109-417) amended PHSA Section
319A to authorize the HHS Secretary to track the initial distribution of federally purchased
influenza vaccine with the voluntary cooperation of vaccine manufacturers, wholesalers, and
distributors during an influenza pandemic.88
Provision
Section 2232 amends PHSA Section 319A to allow the HHS Secretary to track federally
purchased vaccines used in response to other pandemics, in addition to influenza pandemics.
Section 2233: Coordination and collaboration regarding blood supply
Background

84 42 U.S.C. §247d-6.
85 See Congressional Record, vol. 168, no. 42 (March 9, 2022), p. H2673, and CDC, “FY2022 Operating Plan,”
https://www.cdc.gov/budget/documents/fy2022/fy-2022-cdc-operating-plan.pdf.
86 42 U.S.C. §247d-6.
87 42 U.S.C. §247d-7.
88 42 U.S.C. §247d-1.
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The nation’s blood supply is largely managed by a network of independent blood centers and the
American Red Cross.89 These organizations collect blood product donations (e.g., whole blood,
platelets) from individuals through scheduled appointments, walk-in appointments, and blood
drives.
Coordination of blood availability and emergency preparedness is a collaborative effort between
many stakeholders, with input from HHS, FDA, and other federal entities, as well as from
nonfederal partners. The HHS Office of Infectious Disease and HIV/AIDS Policy (OIDP)
supports the coordination of blood safety and emergency preparedness and response activities.
OIDP staff serve as liaisons on a number of councils, task forces, advisory committees, and
programs.90
Provision
Section 2233 requires the Secretary of HHS to ensure coordination and collaboration between
relevant federal departments and agencies related to the safety and availability of the blood
supply. This section specifically requires coordination and collaboration between relevant
agencies within HHS, the Department of Defense (DOD), and the Department of Veterans Affairs
(VA). This section also requires the Secretary to consult and communicate with nonfederal
stakeholders regarding issues related to the safety and availability of the blood supply.
Section 2234: Supporting laboratory capacity and international collaboration to
address antimicrobial resistance
Background
PHSA Section 319E authorized a federal Antimicrobial Resistance Task Force, along with several
activities for addressing antimicrobial resistance (AMR), including research and development for
new drugs and diagnostics, education of health professionals, monitoring at federal health care
facilities, and state-based activities.91 Separately, HHS agencies have many activities to address
AMR that are funded through appropriations but are not specifically named in PHSA Section
319E. For example, CDC established a network of antimicrobial resistance laboratories starting in
2016—a program that currently includes laboratories in all 50 states and several cities.92 HHS
also engages in international collaboration to address AMR.93
Provision
Section 2234 adds a new subsection to PHSA Section 319E that provides formal authorization for
a network of antibiotic resistance regional laboratories to be maintained by CDC, distributed
throughout the United States. These laboratories are to (1) identify and monitor antimicrobial-
resistant pathogens; (2) detect and identify such resistant pathogens, including by providing
support at the request of other laboratories and during emergency responses; and (3) support
diagnosis of resistant pathogens and determine the susceptibility to treatments.

89 For more information on independent blood centers, see https://americasblood.org/about/. For more information on
the American Red Cross, see https://www.redcross.org/give-blood.html.
90 OIDP maintain a list of its roles and responsibilities for the various entities; see https://www.hhs.gov/oidp/topics/
blood-tissue-safety/roles/index.html.
91 42 U.S.C. §247d–5.
92 CDC, “CDC’s Antimicrobial Resistance (AR) Laboratory Networks,” https://www.cdc.gov/drugresistance/
laboratories.html.
93 HHS Office of Global Affairs, “Antimicrobial Resistance,” https://www.hhs.gov/about/agencies/oga/global-health-
security/antimicrobial-resistance/index.html.
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The amended PHSA Section 319E also formally authorizes the HHS Secretary to engage in
international collaboration for addressing AMR, including by (1) supporting research on AMR
pathogens, including those not detected in the United States; (2) supporting surveillance,
laboratory, and other response capacity; and (2) providing technical assistance for AMR infection
control activities. The Secretary may award grants, contracts, or cooperative agreements to public
and private entities, including nongovernmental organizations, for these activities.
Section 2235: One Health framework
Background
The concept of “One Health” recognizes that human health is linked to animal health and the
environment. A One Health approach therefore involves cross-sectoral efforts to address health
challenges such as zoonotic diseases (i.e., diseases that can be transmitted from animals to
humans).94 During the pandemic, CDC established a coordinating committee for One Health
approaches to COVID-19, in collaboration with the U.S. Department of Agriculture (USDA) and
the Department of the Interior (DOI).95 Through appropriations report language (H.Rept. 116-
450), CDC was previously directed to develop a National One Health Framework along with a
standing coordination committee for federal One Health efforts.
Provision
Section 2235 requires CDC, in coordination with other federal departments and agencies, to (1)
develop or update a One Health framework to address zoonotic diseases and advance public
health preparedness, and (2) coordinate with USDA and DOI to develop a One Health
coordination mechanism at the federal level to strengthen One Health collaboration across the
government. The Secretary must report to specified congressional committees no later than one
year after enactment to provide an update on these activities.
Section 2236: Supporting children during public health emergencies
Background
The National Advisory Committee on Children and Disasters (NACCD) is composed of
individuals from both the private and public sector who evaluate issues and programs and provide
advice to the HHS Secretary and the Assistant Secretary for Preparedness and Response on
supporting the preparedness, response, and recovery efforts aimed at the specific needs of
children.96 NACCD was first authorized by the Pandemic and All-Hazards Preparedness
Reauthorization Act of 2013 (PAHPRA, P.L. 113-5) in PHSA Section 2811A97 and was
subsequently reauthorized by the Pandemic and All-Hazards Preparedness and Advancing
Innovation Act (PAHPAIA, P.L. 116-22).
Provision
Section 2236 amends PHSA Section 2811A to include developmental needs among those
evaluated by the National Advisory Committee on Children and Disasters. The provision further
expands the duties of the committee to provide advice and consultation on continuity of care and
education for children, parents, and caregivers during all-hazard emergencies. In addition, this

94 CDC, “One Health Basics,” https://www.cdc.gov/onehealth/basics/index.html.
95 CDC, “Federal One Health Coordination,” https://www.cdc.gov/onehealth/what-we-do/federal-coordination.html.
96 ASPR, “About the National Advisory Committee on Children and Disasters (NAACD),” https://aspr.hhs.gov/
AboutASPR/WorkingwithASPR/BoardsandCommittees/Pages/NACCD/About-Us.aspx.
97 42 U.S.C. §300hh-10b.
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provision updates the composition of the committee to include at least four nonfederal members
representing child care settings, state or local educational agencies, individuals with expertise in
children with disabilities, and parents.
Subtitle C—Accelerating Research and
Countermeasure Discovery
Chapter 1—Fostering Research and Development and Improving
Coordination
Background for Sections 2301-2304
At the onset of the pandemic, researchers in both the public and private sectors undertook efforts
to rapidly study the biology of the virus and to develop new medical products. Prior to the
pandemic, the federal government had established agencies, programs, and responsibilities for
researching and developing new medical countermeasures (MCMs), that is, medical products that
may be used to treat, prevent, or diagnose conditions associated with emerging infectious diseases
or chemical, biological, radiological, or nuclear (CBRN) agents. MCMs include biologics (e.g.,
vaccines, monoclonal antibodies), drugs (e.g., antimicrobials, antivirals), and medical devices
(e.g., diagnostic tests, PPE).98
Agencies involved in MCM R&D include the National Institutes of Health (NIH), the Biomedical
Advanced Research and Development Authority (BARDA), and the Department of Defense
(DOD), among others. Each of these agencies plays a differing, sometimes overlapping, role in
R&D for new MCMs. The PREVENT Pandemics Act primarily addresses NIH’s role in MCM
R&D, particularly the role of the National Institute of Allergy and Infectious Diseases (NIAID)—
the main NIH institute that invests in emerging infectious disease and biodefense research. NIH
and NIAID generally focus on the early stages of R&D for new medical countermeasures,
including basic research to better understand the biology of viruses and immunity, and preclinical
R&D to develop and test potential MCM candidates.99
In addition, the pandemic highlighted other scientific and R&D challenges. In the early stages of
an outbreak with a novel virus, researchers may need access to pathogen samples in order to
study the virus and develop MCMs.100 Many scientists faced challenges gaining access to
pathogen samples in the early stages of the COVID-19 outbreak.101 The pandemic also
highlighted challenges with developing and scaling up diagnostic testing in the early stages of an
outbreak.102 In addition, the pandemic demonstrated the challenge of making health guidance and

98 For additional information, see CRS Report R46427, Development and Regulation of Medical Countermeasures for
COVID-19 (Vaccines, Diagnostics, and Treatments): Frequently Asked Questions.
99 CRS Report R46427, Development and Regulation of Medical Countermeasures for COVID-19 (Vaccines,
Diagnostics, and Treatments): Frequently Asked Questions.
100 Cormac M. Kinsella, Pauline Dianne Santos, Ignacio Postigo-Hidalgo, et al., “Preparedness Needs Research: How
Fundamental Science and International Collaboration Accelerated the Response to COVID-19,” PLOS Pathogens, vol.
16, no. 10 (October 9, 2020).
101 Ewen Callaway, “China Coronavirus: Labs Worldwide Scramble to Analyse Live Samples,” Nature, January 31,
2020, https://www.nature.com/articles/d41586-020-00262-7.
102 U.S. Government Accountability Office, COVID-19: Continued Attention Needed to Enhance Federal
Preparedness, Response, Service Delivery, and Program Integrity, GAO-21-551, July 2021, pp. 17-18,
https://www.gao.gov/assets/gao-21-551.pdf.
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recommendations in the context of a changing novel virus whose health impact is not fully
known. For example, throughout the pandemic, scientists have continued to learn more about
COVID-19 immunity, its durability, and differences between immunity induced by vaccination
compared with infection. COVID-19 immunity has also changed as the virus has evolved over
time.103
Section 2301: Research centers for pathogens of pandemic concern
Provision
Section 2301 adds a new PHSA Section 447D, which authorizes a Research Centers for
Pathogens of Pandemic Concern program to be administered by the National Institute of Allergy
and Infectious Diseases (NIAID). In collaboration with other NIH Institutes and Centers, ASPR,
and BARDA, NIAID is to establish or continue a multidisciplinary research program through
support for research centers to advance the discovery and preclinical development of medical
products for priority virus families and other viral pandemic threats. Funding may be awarded to
public and private entities for (1) conducting basic research through preclinical development of
new medical products; (2) identifying potential targets for therapeutic candidates; (3) identifying
existing medical products with therapeutic potential; and (4) carrying out or supporting other
research related to medical products. NIAID is also to collaborate with other federal departments
and agencies to identify priority virus families and other viral pandemic threats, and with
BARDA to provide updates and identify any advanced R&D needs for medical products
supported by the centers.
Section 2302: Improving medical countermeasure research coordination
Provision
Section 2302 amends PHSA Section 402, which specifies the duties of the NIH Director.104 The
amended PHSA Section 402 requires the NIH Director to consult with ASPR, BARDA, CDC,
and others, as appropriate, regarding research needs to advance medical countermeasures for
public health threats, including emerging infectious diseases and CBRN agents.
Section 2303: Accessing specimen samples and diagnostic tests
Provision
Section 2303 requires the HHS Secretary to issue guidance regarding access to pathogen samples
for research and development. It also adds a new authority, PHSA Section 319B, which addresses
diagnostic test development during emergencies. Within one year after enactment, the HHS
Secretary is required to make publicly available policies and procedures for accessing pathogen
specimens (or other surrogates or alternatives as specified) that support public health
preparedness and response activities, or that support biomedical research for developing and
validating medical products to address emerging infectious diseases. The guidance must include
(1) the method for requesting such samples; (2) considerations for sample availability and use of
suitable surrogates or alternatives to such pathogens, including applicable safeguard and security

103 See, for example, David M. Morens, Gregory K. Folkers, and Anthony S. Fauci, “The Concept of Classical Herd
Immunity May Not Apply to COVID-19,” The Journal of Infectious Diseases, vol. 226, no. 2 (March 21, 2022), pp.
195-198, and COVID-19 Forecasting Team, “Past SARS-CoV-2 Infection Protection Against Re-Infection: A
Systematic Review and Meta-Analysis,” The Lancet, vol. 401, no. 10379 (March 11, 2023), pp. P833-842.
104 42 U.S.C. §282.
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measures; and (3) information required in order to receive such samples or suitable surrogates or
alternatives.
The new PHSA Section 319B allows the HHS Secretary to contract with public and private
entities to increase capacity in the rapid development, validation, manufacture, and dissemination
of diagnostic tests to SLTT health departments and other entities—thereby supporting immediate
public health response activities to address an emerging infectious disease with respect to a PHE
under PHSA Section 319, or to address an emerging infectious disease that has significant
potential to cause such a public health emergency.
Section 2304: National Academies of Sciences, Engineering, and Medicine
study on natural immunity in relation to the COVID-19 pandemic
Provision
Section 2304 requires the HHS Secretary to contract with the National Academies of Sciences,
Engineering, and Medicine (NASEM) to conduct a study related to the current scientific evidence
on the durability of immunity to COVID-19. The study is to include (1) an assessment of
scientific evidence related to the durability of immunity resulting from SARS-CoV-2 infection,
COVID-19 vaccination, or both, including any differences between population groups; (2) an
assessment of the extent to which the federal government makes publicly available the scientific
evidence used by relevant federal departments and agencies to inform public health
recommendations related to immunity resulting from SARS-CoV-2 infection and COVID-19
vaccination; and (3) a summary of scientific studies and evidence related to SARS-CoV-2
infection-acquired immunity from a sample of other countries or multilateral organizations.
NASEM is to submit the report on the study no later than 18 months after enactment to specified
congressional committees. This section does not authorize an appropriation.
Chapter 2—Improving Biosafety and Biosecurity
The provisions set forth in Subtitle C, Chapter 2, of the PREVENT Pandemics Act prescribe a
series of policies and requirements for the executive branch and federal agencies to address
biosafety- and biosecurity-related issues pertaining to research, training, and oversight of life
science research.
The United States has multiple, overlapping policies to manage biosafety and biosecurity issues
associated with emerging technologies and life sciences research. These polices provide guidance
and oversight for life sciences research, depending on the types of experiments and biological
agents used. While some oversight mechanisms are required by law for all public and private
research entities, others are mandatory only if the research is funded by the federal government.
Some biosafety and biosecurity standards are informed by guidance and best practices issued by
federal agencies and other scientific organizations rather than by law. Privately funded research,
or research conducted outside the United States, may therefore not be covered by certain U.S.
oversight mechanisms. Two reports released in 2023 evaluate U.S. polices related to research
with enhanced potential pandemic pathogens (ePPP) and broader biosafety and biosecurity issues
related to life-sciences research: one from the U.S. Government Accountability Office (GAO) and
another from the National Science Advisory Board for Biosecurity (NSABB). Both reports
recommend expanding oversight to include privately funded research. For more information, see
CRS Report R47114, Oversight of Gain of Function Research with Pathogens: Issues for
Congress, and CRS Insight IN12109, Improved Oversight of Pathogen Research: Recent
Recommendations.
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Section 2311: Improving control and oversight of select biological agents
and toxins
Background
The Public Health Security and Bioterrorism Preparedness and Response Act of 2002 (P.L. 107-
188) required HHS to establish and regulate a list of biological agents and toxins that have the
potential to pose a severe threat to public health and safety. The Agricultural Bioterrorism
Protection Act of 2002 (Title II, Subtitle B, of P.L. 107-188) required the U.S. Department of
Agriculture (USDA) to establish and regulate a list of biological agents that have the potential to
pose a severe threat to animal health and safety, plant health and safety, or to the safety of animal
or plant products. These two laws provide the legal basis for the Federal Select Agents Program
(FSAP), managed by the Division of Select Agents and Toxins at the CDC and the Division of
Agriculture Select Agents and Toxins at USDA. CDC and USDA share responsibility for some
agents because they potentially threaten both humans and animals. 42 U.S.C. §262a and 7 U.S.C.
§8401 require CDC and USDA to review and republish the lists of select agents and toxins on at
least a biennial basis.105
FSAP focuses on both the people who have access to select agents and the facilities where select
agents are used and stored. Entities possessing select agents are required under 42 U.S.C. §262a
and 7 U.S.C. §8401 to develop explicit biosecurity and biosafety plans and procedures that are
reviewed and certified by FSAP.106
Provision
The provision amends PHSA Section 351A to further specify who is required by law to have
proper training under the FSAP program.107 This includes individuals who are involved in the
handling and use of select agents and toxins, individuals whose responsibilities routinely put them
in close proximity to laboratory facilities that handle select agents and toxins, and individuals
who perform administrative or oversight functions of facilities that transfer, possess, or use select
agents and toxins.
The provision also makes various amendments to account for risks associated with the accidental
release or theft of agents regulated by FSAP. The provision amends the establishment of
appropriate regulatory safeguards for such agents. In addition to the risk of use in domestic or
international terrorism, the provision expands the scope to include risks posed by the release,
theft, or loss of a select agent or toxin. It requires the HHS Secretary or USDA Secretary to notify
specified committees of any release, loss, or theft of a select agent or toxin reported within 72
hours. Within 14 days after such a notification, an update to such committees is required
describing any actions taken or planned to mitigate the potential threat that the release, loss, or
theft may pose to public health and safety, as well as any actions taken or planned to review the
circumstances of such release, loss, or theft, and to prevent similar events.
The provision also requires an annual report submitted by the Secretary to selected congressional
committees. The report should summarize the number and nature of notifications received,
describe actions taken to address such incidents, and identify any gaps, challenges, or limitations

105 Federal Select Agent Program, https://www.selectagents.gov/sat/index.htm.
106 An entity is defined as any government agency (federal, state, or local), academic institution, corporation, company,
partnership, society, association, firm, sole proprietorship, or other legal entity. An entity is thus not limited to a single
facility or to a single laboratory. An entity may possess one or multiple facilities, each facility containing one or
multiple laboratories.
107 42 U.S.C. §262a
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regarding safety and security practices, as well as actions taken to address such gaps, challenges,
or limitations.
The provision also reauthorizes appropriations for the FSAP program through FY2027.
Section 2312: Strategy for federal high-containment laboratories
Background
CDC and NIH co-publish the Biosafety in Microbiological and Biomedical Laboratories (BMBL)
guidelines, which serve as the overarching guidance document for U.S. biosafety practices for
protecting workers and preventing exposures in biological laboratories. The BMBL provides
guidance for addressing the safe handling and containment of infectious microorganisms and
hazardous biological materials.108 Adherence to the BMBL is a term and condition that some
grant awardees must meet in order to receive funding from certain federal agencies.
The BMBL describes biosafety levels (BSLs), which are designations applied to projects or
activities conducted in laboratories, in ascending order of containment based on the degree of the
health-related risk associated with the work being conducted.109 Each biosafety level (BSL 1-4)
builds upon the previous level. Each level describes a minimum set of safety practices and
procedures, required safety equipment, and administrative and engineering controls. The
appropriate BSL for a research project is determined by the institution in which the work is being
conducted, in consultation with the principal investigator, depending on the specific organism and
types of experiment to be performed. In 2020, 190 entities with BSL-3 laboratories and eight
entities with BSL-4 laboratories were registered with FSAP in the United States, operated by a
variety of actors (federal, commercial, academia, and private).110 Not all of these laboratories are
research labs; for example, they could also include clinical and public health laboratories that deal
with select agents.111
Provision
The provision requires the Director of the Office of Science and Technology Policy (OSTP),
within a year of the enactment, to establish a strategy for the management, maintenance, and
oversight of federally owned laboratory facilities operating at BSL 3 or 4, including equivalent
classification levels and facilities with BSL 4 capabilities. This strategy is to include an
assessment of the needs of the federal government in relation to BSL 3 or 4 laboratories, as well
as a summary of BSL 3 or 4 laboratory capacities established with federal funds but not managed
by the federal government. The strategy is not intended to supersede the current authorities of
relevant federal departments or agencies that have oversight of the management and maintenance
of federally owned or operated facilities.

108 Paul J. Meechan and Jeffrey Potts, Biosafety in Microbiological and Biomedical Laboratories, U.S. Department of
Health and Human Services, 6th Edition, 2020, https://www.cdc.gov/labs/BMBL.html.
109 Department of Health and Human Services, Science Safety Security, https://www.phe.gov/s3/BioriskManagement/
biosafety/Pages/Biosafety-Levels.aspx.
110 Federal Select Agent Program, 2020 Annual Report of the Federal Select Agent Program, 2020,
https://www.selectagents.gov/resources/publications/docs/FSAP_Annual_Report_2020_508.pdf.
111 This is a subset of the total number of BSL 3-4 laboratories in operation; laboratories that do not work with select
agents would not need to register under the Select Agent Program. Therefore, the total number of BSL 3-4 laboratories
may be higher.
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Section 2313: National Science Advisory Board for Biosecurity
Background
The National Science Advisory Board for Biosecurity (NSABB) is a federal advisory committee
governed by the provisions of the Federal Advisory Committee Act.112 The purpose of the
NSABB is to provide, as requested, advice, guidance, and recommendations related to biosecurity
and dual-use research, taking into consideration both national security concerns and the needs of
the research community to foster continued rapid progress in public health and agricultural
research. The NSABB consists of up to 25 voting members with a broad range of expertise. Prior
to the PREVENT Pandemics Act, the NSABB was authorized by 42 U.S.C. §217a, Section 222 of
the Public Health Service (PHS) Act, as amended, and the Pandemic and All-Hazards and
Preparedness Act (P.L. 109-417), Section 205, codified at 42 U.S.C. §262a.113
During its first meeting in 2005, the NSABB was charged with examining the potential
biosecurity concerns raised by the synthesis of select agents and by synthetic biology in general,
and with recommending strategies for addressing these concerns.114 In January 2020, and again in
February 2022, the HHS Secretary charged the NSABB with evaluating and providing
recommendations on the effectiveness of the current oversight frameworks for research involving
enhanced pathogens of pandemic potential and dual-use research of concern.115
Provision
The provision provides a new formal authorization for the NSABB and its role. The provision
amends Part A of Title IV of the Public Health Service Act to add a new Section 404O, which
requires the HHS Secretary, acting though the NIH Director, to establish the NSABB.116 The
provision prescribes the advice that NSABB is to provide. This advice includes oversight of
federally conducted or federally supported dual-use biomedical research, as well as activities
previously prescribed under Section 205 of the Pandemic and All-Hazards Preparedness Act (P.L.
109-417), including advice and recommendations regarding training for workers in high
containment biological laboratories and periodic evaluations of biological laboratory capacity
nationwide. The provision also describes certain strategies to improve the safety and security of
biomedical research that NSABB is to consider. These strategies include leveraging or using new
technologies and scientific advancements to (1) reduce safety and security risks associated with
such research, (2) improve the containment of pathogens, and (3) improve outreach to, and
education and training of, researchers, laboratory personnel, and other appropriate individuals
regarding the safety and security risks associated with such research and mitigation of such risks.
The provision prescribes NSABB’s membership, which is to include voting members appointed
by the HHS Secretary with expertise in biology, infectious diseases, public health ethics, national
security, and other fields, as appropriate. Representatives from several federal departments and
agencies, including HHS, DOD, DHS, and others, are to serve as nonvoting members.

112 National Science Advisory Board for Biosecurity, https://osp.od.nih.gov/biotechnology/national-science-advisory-
board-for-biosecurity-nsabb/#about.
113 National Science Advisory Board for Biosecurity, https://osp.od.nih.gov/policies/national-science-advisory-board-
for-biosecurity-nsabb/.
114 National Science Advisory Board for Biosecurity, https://osp.od.nih.gov/policies/national-science-advisory-board-
for-biosecurity-nsabb#tab3/.
115 National Science Advisory Board for Biosecurity, https://osp.od.nih.gov/biotechnology/national-science-advisory-
board-for-biosecurity-nsabb/#about.
116 42 U.S.C. §281 et seq.
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Section 2314: Research to improve biosafety
Provision
The provision directs the HHS Secretary to conduct or support research to improve the safe
conduct of biomedical research involving pathogens of pandemic potential or agents and toxins
listed under FSAP (PHSA §351A(a)(1)).117 It further requires the Secretary to submit a report
within five years to selected congressional committees on any research conducted or supported,
relevant findings, and steps the Secretary is taking to disseminate those findings.
Section 2315: Federally funded research with enhanced pathogens of
pandemic potential
Background
In January 2017, OSTP released Recommended Policy Guidance for Departmental Development
of Review Mechanisms for Potential Pandemic Pathogen Care and Oversight,118 which described
attributes of federal agency review and reporting processes for the additional oversight of
federally funded research that is anticipated to create, transfer, or use enhanced pathogens with
pandemic potential. HHS soon after released its Framework for Guiding Funding Decisions
about Proposed Research Involving Enhanced Potential Pandemic Pathogens (P3CO).119
Sections III and IV of the HHS P3CO framework establish an additional review process for HHS-
sponsored research proposals that have gone through the normal scientific review process, have
been determined to be scientifically sound, and are reasonably anticipated to create, transfer, or
use ePPP.120 To be subject to this extra scrutiny, an ePPP must satisfy two criteria:
1. It is likely highly transmissible and likely capable of wide and uncontrollable
spread in human populations.
2. It is likely highly virulent and likely to cause significant morbidity and/or
mortality in humans.
If a research proposal meets these criteria, it may be required to go through an independent, HHS-
level, multidisciplinary P3CO review committee.
Based on this review, the P3CO review committee reports to the HHS funding agency (e.g., NIH)
whether the research is acceptable, not acceptable, acceptable on the condition that certain
experiments are modified, or acceptable on the condition that certain risk mitigation measures are
employed at the federal and institutional level. The funding agency makes the final determination
on whether the project will be funded and must report its decision to HHS and OSTP.
Section 19010 of the Coronavirus Aid, Relief, and Economic Security (CARES) Act (P.L. 116-
136) required GAO to examine the extent to which HHS oversight addresses biosafety and
biosecurity risks—including consideration of dual-use research of concern (DURC), FSAP, and

117 2 U.S.C. §262a(a)(1)).
118 Office of Science and Technology Policy, Recommended Policy Guidance for Potential Pandemic Pathogen Care
and Oversight (P3CO), 2017, https://obamawhitehouse.archives.gov/sites/default/files/microsites/ostp/p3co-
finalguidancestatement.pdf.
119 U.S. Department of Health and Human Services, Department of Health and Human Services (HHS) Framework for
Guiding Funding Decisions about Proposed Research Involving Enhanced Potential Pandemic Pathogens , 2017,
https://www.phe.gov/s3/dualuse/Documents/P3CO.pdf.
120 An ePPP is defined as a potential pandemic pathogen resulting from the enhancement of the transmissibility and/or
virulence of a pathogen; which can occur via GOF-type research.
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P3CO—and whether these programs are duplicative. The resulting GAO report, released in
January 2023, made two recommendations related to P3CO and one related to FSAP: 121
• Develop and document a standard for “reasonably anticipated” to ensure
consistency in identifying research for departmental review that is “reasonably
anticipated to create, transfer or use enhanced potential pandemic pathogens.”
• Identify and share nonsensitive information with researchers, Congress, and the
public about the departmental review process for research involving enhanced
potential pandemic pathogens, including information on who is involved in the
review process, their expertise, and how the evaluation criteria are applied.
• When adding a new pathogen to FSAP—which may burden diagnostic and
treatment facilities with additional reporting and inspection requirements—the
Director of the Centers for Disease Control and Prevention should assess and
document the risk posed by the limitations of the existing FSAP exemptions for
public health emergencies and seek legislative authority as needed. Currently,
exemptions are for a maximum of 60 days.
GAO also repeated its recommendation from a 2009 report for HHS to identify a single
government entity to assess the risk posed by the lack of oversight of privately funded research.
In January 2020, and again in February 2022, the Secretary of HHS charged the NSABB with
evaluating and providing recommendations on the effectiveness of the current oversight
frameworks for research involving enhanced pathogens of pandemic potential and dual-use
research of concern. The resulting NSABB report, released in March 2023, made 12
recommendations based on 12 findings from two working groups focused on the implementation
of P3CO and DURC.122 Selected recommendations include the following:
• Clarify definitions of research and expand the scope of biological agents
requiring review under P3CO and DURC.
• Remove certain exclusions for surveillance and vaccine development research.
• Specify roles and responsibilities for investigators and institutions.
• Make P3CO consistent with the 1979 Belmont Report on guidelines for the
protection of human research subjects.
• Monitor for ePPP throughout the entire research life cycle.
• Increase transparency in the review/approval process.
• Ensure equivalent review, evaluation, and ongoing oversight of research funded
at international institutions.
• Engage stakeholders and publishing groups to address information hazards.
• Develop an integrated approach to oversight of research that raises significant
biosafety and biosecurity concerns.
• Expand oversight to nonfederally funded research at institutions and private
companies.

121 U.S. Government Accountability Office, Public Health Preparedness: HHS Could Improve Oversight of Research
Involving Enhanced Potential Pandemic Pathogens, GAO-23-105455, January 2023, https://www.gao.gov/products/
gao-23-105455.
122 National Science Advisory Board for Biosecurity, Proposed Biosecurity Oversight Framework for the Future of
Science, Washington, DC, 2023, https://osp.od.nih.gov/wp-content/uploads/2023/03/NSABB-Final-Report-Proposed-
Biosecurity-Oversight-Framework-for-the-Future-of-Science.pdf.
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The GAO and NSABB reports each provided a separate set of recommendations based on their
findings; however, when considered together, three broad focus areas emerge:123
• Clarifying language and developing standards to identify research that requires
review under the P3CO policy.
• Increasing transparency around the P3CO review and approval processes.
• Expanding oversight to include privately funded research.
Both reports were released after the PREVENT Pandemics Act was enacted into law, and their
findings and recommendations could influence how the provisions of the act are implemented and
interpreted.
Provision
The provision requires the Director of OSTP, in consultation with the heads of relevant federal
departments and agencies, within a year of enactment to conduct a review of existing policies
related to federally funded research “reasonably anticipated to involve the creation, transfer, or
use of enhanced pathogens of pandemic potential.”124 In addition, it requires OSTP to establish or
update policies that would consistently provide review and oversight of such research. Further,
the provision requires OSTP to review and update such policies every four years.
The provision bans the HHS Secretary from funding research involving pathogens of pandemic
potential or biological agents or toxins listed under FSAP by a foreign entity located in a country
of concern, as determined by the Director of National Intelligence or other appropriate federal
agencies. It also allows the Secretary to lift a prohibition on foreign funding under certain
circumstances, and only after notifying Congress prior to lifting the ban.
Chapter 3—Preventing Undue Foreign Influence in Biomedical
Research
Background for Sections 2321-2326
Since 2016, NIH investigations have found issues of foreign influence among its research funding
recipients, including (1) undisclosed sources of foreign research support, (2) undisclosed conflicts
of interest associated with foreign countries and organizations, and (3) violations of the rules and
integrity of the peer review process for NIH funding applications.125 For example, in some cases,
funding recipients received duplicative project funding from a foreign country or organization; in
other cases, peer reviewers shared confidential application information with scientists in foreign
countries.126 An NIH working group found that foreign talent recruitment programs—especially
China’s Thousand Talents program—have encouraged such actions and interference.127
In light of these issues, Congress has funded the HHS Office of the Inspector General (OIG) to
examine NIH’s policies and practices and recommend changes. To date, HHS OIG has explored

123 CRS Insight IN12109, Improved Oversight of Pathogen Research: Recent Recommendations, by Todd Kuiken.
124 Note: The term enhanced pathogens of pandemic potential is and has been used to describe certain types of gain-of-
function research involving both naturally occurring and experimentally induced changes in viruses to better
understand transmission, infection, and pathogenesis.
125 NIH, “About Foreign Interference,” https://grants.nih.gov/policy/foreign-interference/about-foreign-interference.
126 NIH, “About Foreign Interference,” https://grants.nih.gov/policy/foreign-interference/about-foreign-interference.
127 Lawrence A. Tabak and M. Roy Wilson, “Foreign Influences on Research Integrity,” 117th Meeting of the Advisory
Committee to the Director, December 13, 2018, https://acd.od.nih.gov/documents/presentations/
12132018ForeignInfluences.pdf.
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issues related to controls for sensitive genomic research data;128 the vetting process for peer
reviewers;129 financial conflicts of interest policies;130 pre-award risk assessments,131 and
cybersecurity,132 among others. These reports have highlighted potential weaknesses in NIH’s
ability to address security concerns associated with its funded research.
NIH has since amended some of its policies and raised awareness of the issues among funding
recipients.133 In addition, a 2021 presidential memorandum134 and a provision of the William M.
(Mac) Thornberry National Defense Authorization Act for Fiscal Year 2021 (NDAA; P.L. 116-
283, §223) required changes at all federal research agencies to address research security and
disclosure of foreign ties. NIH has made policy changes accordingly.135 Congress also addressed
cross-cutting federal research security issues through P.L. 117-167, commonly referred to the
CHIPS and Science Act, enacted in 2022.136
Issues surrounding the COVID-19 pandemic and investigations into the origins of the virus have
focused attention on NIH’s research security policies. For example, increased attention on NIH’s
funding and oversight of so-called “gain-of-function” research, which can make a virus more
transmissible or pathogenic,137 has invoked broader discussions about oversight of synthetic or
other emerging biology research and its national security implications in general.138 Another
example is increased interest in NIH’s ability to monitor subrecipients of grants located in foreign
countries. For instance, HHS OIG has found that NIH did not effectively monitor funding awards
made to EcoHealth Alliance and its funding subrecipient at the Wuhan Institute of Virology in
China.139
NIH funds research carried out by NIH staff (intramural research) at its own facilities and awards
research funding through grants, contracts, and other agreements to nonfederal entities such as

128 HHS Office of the Inspector General (OIG), Opportunities Exist for the National Institutes of Health to Strengthen
Controls in Place To Permit and Monitor Access to Its Sensitive Data, Audit (A-18-18-09350, February 5, 2019,
https://oig.hhs.gov/oas/reports/region18/181809350.asp.
129 HHS OIG, Vetting Peer Reviewers at NIH’s Center for Scientific Review: Strengths and Limitations, OEI-01-19-
00160, September 25, 2019, https://oig.hhs.gov/oei/reports/oei-01-19-00160.asp.
130 HHS OIG, The National Institutes of Health Has Limited Policies, Procedures, and Controls in Place for Helping to
Ensure That Institutions Report All Sources of Research Support, Financial Interests, and Affiliations, A-03-19-03003,
September 25, 2019, https://oig.hhs.gov/oas/reports/region3/31903003.asp.
131 HHS OIG, The National Human Genome Research Institute Should Strengthen Procedures in Its Pre-Award
Process to Assess Risk for Certain Foreign and Higher Risk Applicants, A-05-20-00026, August 30, 2021,
https://oig.hhs.gov/oas/reports/region5/52000026.asp.
132 HHS OIG, National Institutes of Health Grant Program Cybersecurity Requirements Need Improvement, A-18-20-
06300, September 19, 2022, https://oig.hhs.gov/oas/reports/region18/182006300.asp.
133 NIH, “Foreign Interference,” https://grants.nih.gov/policy/foreign-interference.htm.
134 White House, Presidential Memorandum on United States Government-Supported Research and Development
National Security Policy, National Security Presidential Memorandum - 33, January 14, 2021,
https://trumpwhitehouse.archives.gov/presidential-actions/presidential-memorandum-united-states-government-
supported-research-development-national-security-policy/.
135 NIH, “Requirements for Disclosure of Other Support, Foreign Components and Conflicts of Interest,”
https://grants.nih.gov/policy/foreign-interference/requirements-for-disclosure.
136 See Division B, Title VI, Subtitle D of P.L. 117-167.
137 CRS Report R47114, Oversight of Gain of Function Research with Pathogens: Issues for Congress.
138 CRS Report R47265, Synthetic/Engineering Biology: Issues for Congress.
139 HHS OIG, The National Institutes of Health and EcoHealth Alliance Did Not Effectively Monitor Awards and
Subawards, Resulting in Missed Opportunities to Oversee Research and Other Deficiencies, A-05-21-00025, January
25, 2023, https://oig.hhs.gov/oas/reports/region5/52100025.asp.
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universities (extramural research).140 Other HHS agencies also conduct research and award
funding for medical and health research.
Section 2321: Foreign talent recruitment programs
Provision
Section 2321 requires the HHS Secretary to prohibit NIH intramural research personnel from
participation in foreign talent recruitment programs with some exemptions for international
conferences and programs to be approved by NIH as specified. The Secretary is also required to
make disclosure of foreign talent recruitment program participation a requirement for those
involved in HHS extramural research grants, contracts or other agreements. These requirements
are to be consistent with existing requirements related to foreign talent recruitment programs
established in the CHIPS and Science Act (P.L. 117-167) codified at 42 U.S.C. §19231 et seq.
Section 2322: Securing identifiable, sensitive information and addressing other
national security risks related to research
Provision
Section 2322 requires the HHS Secretary to ensure that NIH and HHS biomedical research is
done in a manner that appropriately considers national security risks, including national security
implications of genomic sequencing and data, as well as identifiable and sensitive information
involved in research, along with the potential misuse of such data. This is to be done in
consultation with the Director of National Intelligence, the Secretary of State, the Secretary of
Defense, and other national security experts. Within two years of enactment, the HHS Secretary is
to develop a comprehensive framework and policies for assessing and managing national security
risks before and after making research funding awards, as well as risks associated with granting
access to data that may pose national security concerns.
One year after developing the comprehensive framework, the HHS Secretary must develop or
implement controls to ensure that (1) researchers have complied with the framework and policies;
(2) funding consideration for projects that may have national security implications takes into
account the extent to which the country involved poses a risk to the integrity of the U.S.
biomedical research enterprise; and (3) committees responsible for reviewing data access requests
for projects that may have national security risks include members with national security
expertise. Data access and sharing policies related to human genomic data are to be updated two
years after developing the comprehensive framework and policies.
The HHS Secretary is required to provide a briefing on these efforts to specified congressional
committees no later than one year after enactment.
Section 2323: Duties of the Director
Provision
Section 2323 amends the duties of the NIH Director as specified in PHSA Section 402.141
Specifically, it adds that the NIH Director is required to (1) consult with the HHS Office of
National Security, ASPR, the Director of National Intelligence, and the FBI Director and others
regarding national security implications of biomedical research conducted or supported by NIH;

140 CRS Report R41705, The National Institutes of Health (NIH): Background and Congressional Issues.
141 42 U.S.C. §282.
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(2) ensure that NIH award recipients and their collaborators (both domestic and nondomestic)
have appropriate technology practices and policies in place to maintain security of identifiable,
sensitive information; and (3) ensure that recipients of NIH awards are in compliance with the
terms and conditions of such award, including through activities to ensure compliance by any
award subrecipients.
Section 2324: Protecting America’s biomedical research enterprise
Provision
Section 2324 requires the HHS Secretary to develop, in consultation with specified federal
national security heads and other experts, a set of strategies and frameworks to protect federally
funded biomedical R&D from national security risks and other threats. The Secretary is to
identify ways to improve protection from national security risks related to (1) intellectual
property, other proprietary information, and identifiable and sensitive information involved in
biomedical R&D; (2) foreign talent programs and countries seeking to exploit U.S. technology
and other proprietary information; (3) national and information security risks associated with the
peer review process; and (4) emerging areas of biomedical R&D that would compromise national
security if subject to undue foreign influence. The Secretary is required to report on such findings
and recommendations to specified congressional committees no later than one year after
enactment.
Section 2325: GAO study
Provision
Section 2325 requires GAO to conduct a study to assess the extent to which HHS provides
funding to entities that use such funds for human genomic sequencing services or genetic
services142 provided by entities organized under the laws of a country (or countries) of concern, as
determined by the Director of National Intelligence or other appropriate agency head. GAO is
required to consider (1) the extent to which countries of concern could obtain genomic
information of U.S. citizens and use such information in a manner inconsistent with the national
security interests of the United States; (2) whether HHS or the funding recipient sought to provide
the funding to a domestic recipient and barriers to the use of domestic entities; (3) whether data
use agreements or other security measures are sufficient to protect the identifiable, sensitive
information of the people of the United States and national security interests. GAO is to make
recommendations to address any national security vulnerabilities identified. GAO is to submit the
report to specified congressional committees no later than two years after enactment in
unclassified form, to the extent practicable, but may include a classified annex.
Section 2326: Report on progress to address undue foreign influence
Provision
Section 2326 requires the HHS Secretary to submit a report to specified congressional
committees no later than one year after enactment on actions taken to (1) address cases of
noncompliance with disclosure requirements or research misconduct related to foreign influence,
including the number of noncompliance cases investigated by or reported to NIH and the number
of cases referred to HHS OIG and other intelligence agencies, along with enforcement actions

142 “Genetic services” as defined in the Genetic Information Nondiscrimination Act of 2008 (42 U.S.C. §2000ff(6)).
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taken; and (2) prevent, address, and mitigate instances of noncompliance with disclosure
requirements or research misconduct related to foreign influence.
Chapter 4—Advanced Research Projects Agency–Health
Section 2331: Advanced Research Projects Agency–Health
Background
Through FY2022 appropriations (P.L. 117-103), Congress provided $1 billion to establish the
Advanced Research Projects Agency for Health (ARPA-H) at HHS. ARPA-H advances “high-
potential, high-impact biomedical and health research that cannot be readily accomplished
through traditional research or commercial activity.”143 First proposed in the Biden
Administration’s FY2022 budget request for NIH, ARPA-H is modelled after other “ARPAs” in
the federal government, especially the Defense Advanced Research Projects Agency. In 2022, the
HHS Secretary established ARPA-H within NIH, with its Director reporting to the HHS
Secretary.144
Throughout 2022, both the House and Senate considered separate bills to authorize ARPA-H. In
the Senate, the PREVENT Pandemics Act (S. 3799, as amended in committee) incorporated the
previously introduced Advanced Research Project Authority for Health Act (S. 3819) as Section
331. In the House, H.R. 5585 was passed on June 22, 2022. The two bills differed primarily in
ARPA-H’s placement within HHS and the means of ensuring its independence. Independence at
the agency level to shape a distinct mission and culture, along with autonomy of program
managers to select and fund projects, are viewed as key components of the ARPA model.145 H.R.
5585 would have made ARPA-H an independent agency within HHS; S. 3819 would have placed
the new agency within NIH with some provisions aimed at creating independence from other NIH
programs. For more information on ARPA-H, see CRS Report R47568, Advanced Research
Projects Agency for Health (ARPA-H): Overview and Selected Issues.
Provision
Section 2331 establishes ARPA-H as focused on driving breakthroughs in biomedical science and
medicine. It also grants the agency many of the common authorities and flexibilities provided to
other ARPA agencies, such as hiring flexibilities and funding authorities (e.g., other transaction
authorities). The authorization includes the following key provisions:
• ARPA-H is established as a part of NIH. The ARPA-H Director reports directly
to the HHS Secretary.
• ARPA-H is required to have offices or facilities in at least three geographic areas.
ARPA-H cannot be located on NIH’s existing campus.
• The Director is to ensure that staff have not worked at NIH in the prior three
years, but can grant an exemption for individuals who are uniquely qualified to
advance ARPA-H’s goals.
• ARPA-H is to prioritize awards to domestic recipients and cannot award funding
to nondomestic recipients organized under the laws of Russia, Iran, North Korea,

143 ARPA-H, FY2024 Congressional Justification, p. 6, https://arpa-h.gov/assets/files/ARPA-H_FY_2024.pdf.
144 CRS Report R47074, Advanced Research Projects Agency for Health (ARPA-H): Congressional Action and
Selected Policy Issues.
145 Azoulay et al., “Funding Breakthrough Research: Promises and Challenges of the ‘ARPA Model,’” pp. 9-10.
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China, or other countries determined to be a covered foreign country under
Section 119C of the National Security Act of 1947.
Subtitle D—Modernizing and Strengthening the
Supply Chain for Vital Medical Products
The COVID-19 pandemic affected the medical product supply chain globally and domestically.
Although concerns about the U.S. medical product supply chain predate the emergence of
COVID-19, the pandemic underscored the importance of understanding, developing, and
protecting the medical product supply chain. The sections within this subtitle address several of
the concerns noted by stakeholders146 during the pandemic, including reducing U.S. reliance on
foreign sources of medical products, increasing the federal government’s ability to oversee the
supply chain and mitigate future disruptions, providing enhancements to the Strategic National
Stockpile (SNS), and increasing production of critical medical products.
Section 2401: Warm-base manufacturing capacity for medical countermeasures
Background
Within ASPR, the Biomedical Advanced Research Development Authority (BARDA) coordinates
and supports the advanced research, development, manufacturing, and initial procurement of
medical countermeasures for use in emergency situations. Established in 2006 by the Pandemic
and All-Hazards Preparedness Act (PAHPA, P.L. 109-417), BARDA collaborates with public and
private sector stakeholders to achieve its mission.
Warm-base manufacturing refers to the capacity of a manufacturing facility to rapidly produce
critical medical countermeasures for use during a public health crisis. Improving this capacity
involves the research, utilization, and incorporation of advanced manufacturing and platform
technologies in existing and new manufacturing facilities.147
Provision
Section 2401 contains several amendments to PHSA Section 319L148 focusing on enhancing
domestic surge manufacturing capabilities and capacity related to certain products. Specifically,
this provision directs BARDA to take the following actions:
• Support, maintain, and improve domestic manufacturing surge capacity and
capability to increase the availability of medical countermeasures for use in
public health crises.
• Facilitate communication between various private and public stakeholders
regarding the development of domestic manufacturing capabilities with regard to
various medical countermeasures.
• Authorize BARDA to award contracts, grants, and other cooperative agreements
or enter into other transactions to support domestic manufacturing surge capacity
and capabilities through the use of advanced manufacturing techniques. Among

146 See, for example, CRS Report R46507, FDA’s Role in the Medical Product Supply Chain and Considerations
During COVID-19.
147 GAO, HHS Has Funded Flexible Manufacturing Activities for Medical Countermeasures, but It Is Too Soon to
Assess Their Effect, March 2014, p. 10, https://www.gao.gov/assets/gao-14-329.pdf.=10.
148 42 U.S.C. §247d-7e.
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other requirements, award recipients are required to annually submit reports on
the maintenance of these capacities and to ensure their ability to rapidly
manufacture countermeasures as required by the Secretary.
• Direct BARDA to consult with the FDA to ensure that manufacturing facilities,
pursuant to these grants, are including current good manufacturing practices.
In addition, this provision extends the authorization for BARDA’s Medical Countermeasure
Innovation Partner program through FY2028.
Strategic National Stockpile: Sections 2402-2409
Background for Sections 2402-2409
The Strategic National Stockpile (SNS) is an inventory of medical countermeasures that can be
deployed to state, local, tribal, and territorial (SLTT) jurisdictions for use in emergencies when
existing supplies are depleted or unavailable. The SNS formulary contains a wide range of
products to respond to a variety of different hazards. The HHS Secretary is statutorily required149
to conduct an annual threat-based review of the products within the SNS to assess whether they
are consistent with the recommendations issued by the Public Health Emergency Medical
Countermeasures Enterprise (PHEMCE).150 The HHS Secretary is also required to adhere to
several procedures to ensure the contents, security, and the safe deployment of the products
within the SNS.151
SLTT health officials may request emergency medical countermeasures (such as antibiotics,
antitoxins, medical supplies and equipment) from the SNS. These requests can be placed through
select officials in these jurisdictions. During the COVID-19 pandemic, existing guidance and
policies detailing how SLTT stakeholders could access supplies were somewhat dated.152 Tribes,
tribal organizations, and urban Indian organizations reportedly had difficulties accessing PPE and
other materials, including through the SNS.153 Officials in these jurisdictions reportedly were
sometimes unable to request supplies directly from the SNS and instead coordinated their efforts
with state or territorial health officials as directed by the ASPR.154
The SNS employs several methods to manage stockpile assets, including vendor-managed
inventory (VMI). Under the VMI program, SNS pays vendors to store and manage some SNS
supplies. This arrangement allows a vendor to rotate its product through this inventory on its way
to other commercial markets to prevent expiration of the product. Delivery of supplies from
vendor-managed inventory takes between 24 and 36 hours.155
Currently, state, local, tribal, and territorial governments are not required to maintain their own
stockpile of medical and ancillary equipment to prepare for and respond to localized emergencies.
State, local, and territorial health jurisdictions may choose to use funding from federal grant

14942 U.S.C. §247d-6b(2).
150 The PHEMCE is a United States interdepartmental committee that facilitates the coordination of the research,
development, and procurement of medical countermeasures in response to emergency situations. 42 U.S. Code
§300hh–10a
151 42 U.S.C. §247d-6b.
152 See CDC, Receiving, Distributing and Dispensing Strategic National Stockpile Assets: A Guide to Preparedness,
Version 11, https://www.orau.gov/sns/v11/ReceivingDistributingDispensingSNSAssets_V11.pdf.
153 “Senate Indian Affairs Committee Holds Hearing on Native American Health During the New Coronavirus,” July 1,
2020, https://plus.cq.com/doc/congressionaltranscripts-5947593?0&searchId=DNWVg7bB.
154 See CRS Report R47400, The Strategic National Stockpile: Overview and Issues for Congress.
155 Ibid.
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programs to stockpile medical countermeasures and prepare for sub-state distribution of stockpile
materials.156
Sections 2402 to 2409 contain several amendments to existing programs and authorizations for
novel programs, which overall are designed to improve SNS inventory management, increase
visibility, and enhance distribution of SNS contents.
Section 2402: Supply chain considerations for the Strategic National Stockpile
Provision
This provision directs the HHS Secretary to consider the impact that the addition, modification, or
replenishment of MCMs in the SNS may have on the availability of those products or ancillary
medical supplies. This provision also directs the HHS Secretary to conduct an assessment of the
entire supply chain for these products, as directed.
Section 2403: Strategic National Stockpile equipment maintenance
Provision
Section 2403 amends PHSA Section 319F-2(a)(3) to require the HHS Secretary to also consider,
among other items, that the contents of the stockpile are in working condition and ready for
deployment.157
Section 2404: Improving transparency and predictability of processes of the
Strategic National Stockpile158
Provision
Section 2404 requires the HHS Secretary, within 60 days of enactment, to issue guidance
describing the process by which the Secretary deploys SNS contents. This guidance must include
information related to the process by which entities request SNS contents, facts considered by the
Secretary when making distribution decisions, and points of contact that requesting entities may
use for information related to SNS requests and received materials.
Further, this section amends PHSA Section 319F-2(a)(3) to add a new subsection that requires the
Secretary to convene meetings with SLTT jurisdictions, relevant industry, federal agencies, and
other stakeholders to coordinate and share information related to maintenance and use of the
SNS.159
Section 2405: Improving supply chain flexibility for the Strategic
National Stockpile
Provision
Section 2405 amends PHSA Section 319F-2 to authorize the HHS Secretary to execute contracts
or cooperative agreements for vendor-managed inventory (VMI) of stockpiled supplies.160 The

156 Ibid.
157 42 U.S.C. §247d-6b(a)(3).
158 As of the date of publication of this report, this guidance is now available. See, ASPR, “Requesting SNS Assets,”
https://aspr.hhs.gov/SNS/Pages/Requesting-SNS-Assets.aspx.
159 42 U.S.C. §247d-6b(a)(3).
160 42 U.S.C. §247d-6b.
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amended section gives the Secretary the authority to dictate the terms and conditions of such
contracts with respect to procurement, maintenance, storage, and delivery of stockpiled items, and
maintenance of domestic manufacturing capacity of such products. This section also directs the
HHS Secretary to issue a report to Congress no later than two years after enactment on VMI
contracts and cooperative agreements, which must include the amount and recipient of each
award, the products covered through the award, and how the Secretary works with recipients to
ensure the situational awareness of manufacturing capacity and inventory of such products. This
section also amends the requirement for a GAO report so that an assessment of VMI contracts is
included in the report. The provision also sets a deadline of March 15 of each year for annual
notice to Congress on the determination of material threats. Lastly, this section authorizes SNS
appropriations of $610 million for each of FY2019 and FY2021, and $750 million for each of
FY2022 and FY2023.
Section 2406: Reimbursement for certain supplies
Provision
Section 2406 amends PHSA Section 319F-2(a) to amend the process for selling surplus or
expiring supplies in the SNS.161 This section states that the Secretary may make SNS contents
available for purchase only if (1) the contents are in excess of what is required for appropriate
stockpile maintenance, (2) the costs for maintaining such excess are not appropriate to meet the
needs of the stockpile, and (3) making such supplies available for purchase does not compromise
national security. This section further dictates the reimbursement and collection mechanisms that
may be implemented by the Secretary to reimburse for the cost of acquiring and maintaining such
supplies. This section also requires the HHS Secretary to issue a report to Congress within two
years of enactment, and annually thereafter, on the use of this authority. This authority sunsets on
September 30, 2028.
Section 2407: Action reporting on stockpile depletion
Provision
Section 2407 amends PHSA Section 319 by requiring the Secretary to submit a report to
Congress no later than 30 days after a deployment of SNS contents in response to an incident, and
every 30 days thereafter until the expiration of such incident(s), on the stockpile deployment, the
contents that remain in the stockpile following deployment, and plans to replenish the
stockpile.162
Section 2408: Provision of medical countermeasures to Indian programs
and facilities
Provision
Section 2408 amends PHSA Section 319F-2(a)(3) by specifying that the Secretary will consult
with and provide assistance to tribal officials, as well as state and local officials, related to the
SNS.163 This section also establishes a new PHSA section (319F-5) that requires the Secretary to
make SNS contents available directly to Indian tribes and tribal organizations.

161 42 U.S.C. §247d-6b(a).
162 42 U.S.C. §247d.
163 42 U.S.C. §247d-6b(a)(3).
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Section 2409: Grants for State strategic stockpiles
Provision
Section 2409 amends Section 319F-2 of the PHSA to establish a pilot program to support state
medical countermeasure stockpiles.164 These grants are to be administered by the Secretary in
consultation with the ASPR and the CDC Director, and to support not fewer than five states or
consortia of states in establishing, expanding, or maintaining a stockpile of drugs, vaccines,
biological products, medical devices, and other medical materials determined by the grantee to be
necessary to respond to a public health emergency, emergency, or major disaster. Funds may not
be used to stockpile security countermeasures, unless approved by the Secretary. Grantees must
agree to a nonfederal contribution ratio through FY2023 to FY2025 and thereafter as specified.
Awards made under this authority are meant to supplement, not supplant, the use of the SNS.
This section also requires the Secretary to issue guidance and technical assistance related to
maintaining and replenishing stockpiles, including strategies and best practices related to types of
materials to be stockpiled, stockpile management procedures, and procurement requirements.
Grantees must submit an annual report to the Secretary on the implementation of the plan
required by this statute, and the Secretary must submit an annual report to Congress on the
program. This section authorizes appropriations of $3.5 billion for each of FY2023 and FY2024,
to remain available until expended. Finally, this section requires a GAO report on the state
stockpiles established pursuant to this section no later than three years after the first awards under
this section are issued.
Domestic medical supply manufacturing: Sections 2410-2411
Background for Sections 2410-2411
Throughout the COVID-19 pandemic, the drug supply chain faced several issues, including
shortages of raw materials, disruptions in manufacturing, and transportation challenges. These
issues were caused by a combination of factors, including factory shutdowns, border closures, and
increased demand for certain medications.165 As a result, some stakeholders have stated that using
domestic production of certain medications, among other actions, may reduce reliance on foreign
products during public health crises and strengthen the drug supply chain.166
Section 2410: Study on incentives for domestic production of generic
medicines
Provision
Section 2410 requires the HHS Secretary, acting through the Assistant Secretary for Planning an
Evaluation (ASPE) to conduct a study on the feasibility, sustainment, potential effectiveness, and
utility of providing incentives for increased domestic product and capacity of specified generic
drugs and their active pharmaceutical ingredients not later than one year after the enactment of
this act.

164 42 U.S.C. §247d-6b.
165 Mariana P. Socal, Joshua M. Sharfstein, and Jeremy A. Greene, “The Pandemic and the Supply Chain: Gaps in
Pharmaceutical Production and Distribution,” American Journal of Public Health, vol. 111, no. 4 (April 2021), pp.
635-639, https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7958046/.
166 See, for example, FDA, “Executive Order 13944 List of Essential Medicines, Medical Countermeasures, and
Critical Inputs,” https://www.fda.gov/about-fda/reports/executive-order-13944-list-essential-medicines-medical-
countermeasures-and-critical-inputs.
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Section 2411: Increased manufacturing capacity of certain critical
antibiotic drugs
Provision
Section 2411 authorizes the HHS Secretary, in consultation with the ASPR and the FDA, to award
contracts to increase the domestic manufacturing capacity of certain antibiotic drugs (or their
active pharmaceutical ingredients or key starting materials) with identified supply chain
vulnerabilities. These grants shall be eligible to certain drug manufacturers after submission of an
application that includes elements such as the manufacturer’s strategic plan for achieving,
maintaining, and sustaining increased manufacturing facilities. Grantees are to be required to
submit follow-up reports as required by the HHS Secretary. The HHS Secretary is to be required
to submit a biennial report on any activities authorized under this provision, as specified. This
authority is to cease to be effective three years after the enactment and have no force or effect
three years after enactment.
Subtitle E—Enhancing Development and
Combating Shortages of Medical Products
At the onset of the pandemic, few treatment options were available for COVID-19 and no
vaccines were available to prevent the disease. Increased demand for personal protective
equipment (PPE) and other medical supplies disrupted medical product supply chains, resulting in
shortages. This situation highlighted larger issues about U.S. reliance on foreign sources of
medical products and the federal government’s ability to oversee the supply chain and mitigate
future disruptions.167 The U.S. Food and Drug Administration (FDA), the focus of this subtitle, is
the primary federal agency responsible for regulating most medical products and has key
responsibilities in responding to medical supply shortages.
A critical part of the COVID-19 public health response was the development new MCMs to
address COVID-19, including biologics (e.g., vaccines, monoclonal antibodies), drugs (e.g.,
antimicrobials, antivirals), and medical devices (e.g., diagnostic tests, PPE).168 Medical product
development and regulatory review is a difficult and high-risk endeavor that takes years in typical
circumstances. In response to public health emergencies, federal law allows certain aspects of
medical product development and review to be expedited. Expedited medical product
development and review also carries certain potential risks, such as a more limited safety profile
for new products upon authorization. In the context of a health emergency such as a pandemic,
and pursuant to its authority, FDA evaluates the risks and benefits of introducing new or modified
products to the market on an abbreviated timeline.169
In addition, FDA plays a key role in monitoring and addressing medical supply shortages,
although its authority varies by product type. Various stakeholders have noted that during the
COVID-19 pandemic, a number of overlapping factors (e.g., unexpected demand spike increases

167 For additional information, see CRS Report R46628, COVID-19 and Domestic PPE Production and Distribution:
Issues and Policy Options; CRS Report R46507, FDA’s Role in the Medical Product Supply Chain and Considerations
During COVID-19; and CRS In Focus IF11488, Personal Protective Equipment (PPE) and COVID-19: FDA
Regulation and Related Activities.
168 For additional information, see CRS Report R46427, Development and Regulation of Medical Countermeasures for
COVID-19 (Vaccines, Diagnostics, and Treatments): Frequently Asked Questions.
169 CRS Report R46427, Development and Regulation of Medical Countermeasures for COVID-19 (Vaccines,
Diagnostics, and Treatments): Frequently Asked Questions.
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for certain medical products, disruptions to the medical supply chain, and global trade
interruptions) led to acute medical product shortages.170
Chapter 1—Development and Review
Throughout the COVID-19 pandemic, stakeholders expressed concern at the lack of novel
therapies to treat COVID-19.171 FDA regulates the safety, effectiveness, and quality of MCMs
through premarket and postmarket activities. With respect to its premarket work, FDA granted
marketing approval, clearance, and emergency use authorization (EUA) to COVID-19
therapeutics, vaccines, diagnostics, and other medical devices (e.g., respirators and ventilators).172
In addition, FDA issued numerous guidance documents to facilitate COVID-19 MCM
development and marketing authorization.
A number of regulatory flexibilities were utilized during the COVID-19 pandemic to both
encourage the development of novel medical countermeasures and accelerate the review process
for these products so they could be more quickly deployed. This chapter includes a number of
provisions that encourage and enhance the ability of the FDA to safely accelerate product
development and review.
Section 2501: Accelerating countermeasure development and review
Background
Section 565 of the Federal Food, Drug and Cosmetic Act (FFDCA) outlined the responsibility of
the HHS Secretary, in consultation with the ASPR, to ensure appropriate involvement of the FDA
with accelerating the development, stockpiling, approval, licensure, and clearance of
countermeasures.173 These responsibilities included promoting expertise and situational
awareness within the FDA, developing specialized teams within the FDA with expertise on
countermeasures, and providing technical assistance to manufacturers and others. Prior to the
PREVENT Pandemics Act, FDA did not have specific authority to expedite the development or
review of such countermeasures, though FDA used some of its existing regulatory mechanisms to
expedite review of COVID-19 products during the pandemic.174
Provision
Section 2501 amends FFDCA Section 565 to add a new subsection that authorizes the HHS
Secretary, at his or her discretion and at the request of a countermeasure sponsor during specified
incidents, to take certain actions to expedite the development and review of countermeasures for
approval, licensure, clearance, or authorization of products. These actions may include expedited
review of sponsor submissions, expedited and increased sponsor engagement, and expedited
issuance of guidance to industry stakeholders.

170 Johns Hopkins University, The Pandemic and The Supply Chain: Addressing Gaps in Pharmaceutical Production
and Distribution, November 2020, https://www.jhsph.edu/research/affiliated-programs/johns-hopkins-drug-access-and-
affordability-initiative/publications/Pandemic_Supply_Chain.pdf.
171 Phillip C. Robinson, David F.L. Liew, Helen L. Tanner, et al., “COVID-19 Therapeutics: Challenges and Directions
for the Future,” PNAS, vol. 119, no. 15 (March 1, 2022).
172 FDA, Emergency Use Authorization, “Coronavirus Disease 2019 (COVID-19) EUA Information,”
https://www.fda.gov/emergency-preparedness-and-response/mcm-legal-regulatory-and-policy-framework/emergency-
use-authorization#covid19euas.
173 21 U.S.C. §360bbb-4.
174 See FDA, “Coronavirus Treatment Acceleration Program,” https://www.fda.gov/drugs/coronavirus-covid-19-drugs/
coronavirus-treatment-acceleration-program-ctap.
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Section 2502: Third-party test evaluation during emergencies
Background
During the COVID-19 pandemic, FDA relied on its Emergency Use Authorization (EUA)
authority to increase access to many medical products.175 This authority enabled access to
numerous medical products, but particularly to COVID-19 tests, in an expedited manner, using
abbreviated requirements for marketing authorization.176 More than 400 COVID-19 tests received
EUA during the pandemic, including molecular diagnostic, antigen, and serology tests, among
others. The volume of EUA submissions was said to be challenging for the agency during a time
when it was prioritizing many other COVID-19-related review activities.
Provision
Section 2502 adds a new FFDCA Section 565(i) to allow the Secretary to consult or enter into
cooperative agreements with experts when evaluating in vitro diagnostics that are the subject of
EUA submissions to determine whether they meet the criteria for EUA issuance. These experts
may conduct evaluations and provide recommendations relating to the scope and conditions of
the authorization. In so doing, they must consider whether the diagnostic meets the conditions in
FFDCA Section 564(c)(2) for issuance of an EUA, and recommendations must be submitted to
the Secretary in writing. Not later than one year after enactment, the HHS Secretary is required to
publish draft guidance on the consultations occurring under Section 565(i), including
considerations around compensation and conflict of interest, among others. A revised draft or
final guidance must be published not later than one year after public comment closes for the
initial draft guidance.
Section 2503: Platform technologies
Background
Platform technologies are tools that can be adapted and reused to develop a range of medical
products, including drugs, vaccines, and diagnostics. Use of these technologies may reduce the
time and cost required to develop subsequent products.177 The FDA has recognized the potential
benefits of platform technologies in drug development and has encouraged their use through
various initiatives and policies.178
Provision
This provision adds a new section in the FFDCA (FFDCA §506K) that establishes a program for
the designation of certain technologies as platform technologies under certain conditions, such as
• the technology is used in the development of certain drug products;

175 See generally FFDCA §564 (21 U.S.C. §360bbb-3).
176 The criteria for issuing an EUA are found at FFDCA §564(c)(2) and include, for example, that based on the totality
of scientific evidence, the product being evaluated may be effective in treating or preventing the disease that is the
subject of the emergency, and that the known and potential benefits of the product outweigh the known and potential
risks of the product.
177 Michael Siedler, “Implementation of a Platform Approach for Early Biologics Development,” American
Pharmaceutical Review, September 1, 2011, https://www.americanpharmaceuticalreview.com/Featured-Articles/
37325-Implementation-of-a-Platform-Approach-for-Early-Biologics-Development/.
178 FDA, “Emerging Technology Program,” last updated Nov. 14, 2022, https://www.fda.gov/about-fda/center-drug-
evaluation-and-research-cder/emerging-technology-program.
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• preliminary evidence suggests that the technology has the potential to be used in
multiple drug products; and
• data suggest that the technology has a reasonable likelihood to bring significant
efficiencies to the drug development, manufacturing, and review processes.
An individual or product sponsor may request designation of a platform technology either with or
at any time during a drug product submission that uses this technology. Upon receipt of the
request, the Secretary shall determine whether the technology meets the specified criteria for the
designation. Upon such a determination, the Secretary may take certain actions to expedite the
development and review of an application that uses this technology, including engaging with
sponsors early, providing timely advice to drug sponsors, and considering inspectional findings
that incorporate the use of such technology. The HHS Secretary may also choose to not designate
a technology as a platform technology, or to revoke an earlier designation.
The Secretary must allow the sponsor of a drug application to reference data from another
application that uses the same platform technology. Sponsors of multiple approved drug products
that incorporate or use a designated platform technology may submit a single supplemental
application for proposed changes to the technology that may be applicable to other products using
the same technology.
The Secretary must also issue draft guidance on the implementation of this section not later than
one year after the date of enactment and must issue a report not later than September 30, 2026,
and annually for the next three years on the number of platform technology designations,
resources used, and efficiencies gained, among other program metrics.
Section 2504: Increasing EUA decision transparency
Background
During the COVID-19 pandemic, FDA used EUAs to make a variety of medical products
available. GAO has noted that although FDA’s EUA decisions are communicated via
authorization letters and subsequent publicly available data, the underlying evidence that FDA
used to support its authorization has not always been transparent.179 FDA noted that it had tried to
improve its transparency regarding EUA decisions, but that certain federal laws may have limited
what information the agency was able to share.180 Prior to the PREVENT Pandemic Act, Section
564(h) of the FFDCA181 required that FDA publish a notice of EUA authorization, termination or
revocation for certain product classes in the Federal Register.
Provision
Section 2504 amends the existing FDA requirement to publish a notice of each EUA
authorization, termination, or revocation in FFDCA Section 564(h). 182 Specifically, the section
broadens the types of products for which notices are required. The provision also directs the
Secretary to make any EUA revisions available on an FDA website, which may include a

179 GAO, Federal Efforts Accelerate Vaccine and Therapeutic Development, but More Transparency Needed on
Emergency Use Authorizations, November 2020, p. 29, https://www.gao.gov/assets/gao-21-207.pdf.
180 Ibid. at 33.
181 21 U.S.C. §360bbb-3(h).
182 21 U.S.C. §360bbb-3(h).
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summary of the data and information supporting such revisions. The provision also clarifies that
EUA revisions and accompanying documents are authorized disclosures under federal law.183
Section 2505: Improving FDA guidance and communication
Background
FDA regularly communicates with the public and other stakeholders through various publications,
including guidance documents and external stakeholder (including product sponsor)
communications.184 Though FDA guidance documents are nonbinding, they represent FDA’s
current policy interpretations regarding regulatory issues.185 Communications with external
stakeholders may include, for example, correspondence with product sponsors developing novel
medical products.186
In a 2021 policy brief, Senator Burr noted that “[d]uring the COVID-19 public health emergency,
FDA quickly published guidance and other regulatory documents” that “helped speed the
development and availability of medical countermeasures to turn the tide on the pandemic
response.”187 Consequently, the brief recommended that FDA strengthen its regulatory readiness
by “adopt[ing] [its] best practices that emerged during the pandemic related to providing
guidance to and interacting with sponsors” to increase future communication speed and
transparency.188
Provision
Section 2505 stipulates that the Secretary shall develop and publish a report detailing best
practices for guidance document prioritization, development, issuance, and use across FDA and
other applicable agencies. In addition, the Secretary shall develop and publish an implementation
plan that addresses streamlining guidance document creation and FDA regulatory submission
processes, implementing innovative guidance measures, and transitioning or updating appropriate
guidance issued during COVID-19.
The Secretary shall also develop and publish a report detailing FDA’s nonguidance document
communication practices with external stakeholders. The report shall include a review of the
types and methods of these communications, related best practices, and a corresponding
implementation plan, with further details as specified. The Secretary shall consult with
stakeholders, as specified, pursuant to the development and publication of the reports and
implementation plans.
In fulfilling these responsibilities, the Secretary may update an existing report or plan, and may
further combine the reports and implementation plans discussed above into one or more
documents. Within one year of enactment, the Secretary must publish a draft of the reports and

183 Specifically 18 U.S.C. §1905.
184 For FDA’s regulations governing guidance documents, see generally 21 C.F.R. §10.115, and FDA, “Guidances,”
January 24, 2022, https://www.fda.gov/industry/fda-basics-industry/guidances.
185 Ibid.
186 See, for example, FDA, CDER, CBER, Best Practices for Communication Between IND Sponsors and FDA During
Drug Development: Guidance for Industry and Review Staff, December 2017, pp. 3-5, at https://www.fda.gov/media/
94850/download.
187 Richard Burr, Strengthening FDA’s Regulatory Readiness: Implementing Lessons Learned from the COVID-19
Pandemic, policy brief, September 30, 2021, p. 3, at https://www.help.senate.gov/imo/media/doc/
Burr%20Policy%20Brief%20-%20Strengthening%20FDA's%20Regulatory%20Readiness.pdf.
188 Ibid., pp. 5-6.
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plans, and no later than 180 days following the draft publications, the Secretary must publish a
final report and plan and begin implementing plan best practices.
Chapter 2—Mitigating Shortages
As the federal regulator of drugs and devices, FDA plays a critical role in overseeing aspects of
the U.S. medical product supply chain. Drug and device manufacturers are required, by law, to
report to FDA certain supply chain-related information, with some exceptions for emergency
circumstances. For example, establishments that manufacture drugs and devices are required to
register with FDA and list the drugs and devices they manufacture for U.S. commercial
distribution. This registration helps FDA maintain a catalog of all drugs, biologics, and devices in
commercial distribution in the United States. FDA relies on establishment registration and listing
information to carry out various programs and activities, including establishment inspections,
postmarketing surveillance, recalls, drug quality reports, adverse event reports, monitoring of
drug and device shortages and availability, supply chain security, and identification of products
marketed without an approved application.
To enhance FDA’s capacity to assess the medical product supply chain and device manufacturing,
Congress created requirements for reporting drug and device manufacturing interruptions and for
tracking drugs as they are distributed to consumers. To help prevent and mitigate shortages,
manufacturers of certain drugs and devices must notify FDA of any interruptions or
discontinuances in their manufacturing. FDA is required to take certain mitigating actions in
response to such notification. For example, FDA must prioritize and expedite facility inspections
and review of certain regulatory submissions. Notably, drug manufacturers are required to report
such interruptions or discontinuances at any time, whereas device manufacturers are subject to
this requirement only in the context of a public health emergency.
In addition, to make the public aware of supply chain disruptions, FDA is required by law to
maintain public, up-to-date lists of drugs and devices that are in short supply. FDA publishes
these lists based on the information it receives from various entities.189
Section 2511: Ensuring registration of foreign drug and device manufacturers
Background
FDA upholds registration requirements for manufacturers of the various medical products that it
regulates.190 Although these requirements have granted the FDA some insight into the medical
supply chain, numerous stakeholders have reported data gaps. These gaps, they say, have
consequently made monitoring product development throughout the manufacturing lifecycle a
challenge.191
Provision
Section 2511 amends FFDCA Section 510(i) to expand the requirement for certain foreign drug
and device manufacturers to register with the United States, specifying that the registration
requirements stated therein are applicable regardless if the product undergoes further preparation,
propagation, compounding, or processing at a separate foreign facility prior to importation or

189 CRS In Focus IF11058, Drug Shortages: Causes, FDA Authority, and Policy Options.
190 FDA, “Registration and Listing,” last updated February 2, 2023 at https://www.fda.gov/industry/fda-basics-industry/
registration-and-listing.
191 For more details, see CRS Report R46507, FDA’s Role in the Medical Product Supply Chain and Considerations
During COVID-19, at p. 20.
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offer for importation within the United States.192 This section also directs the HHS Secretary to
update appropriate regulations to implement the updated registration requirements.
Section 2512: Extending expiration dates for certain drugs
Background
Federal regulations require that the expiration dates for drug products are determined by
appropriate stability testing.193 These expiration dates reflect the period of time in which a drug
product retains its medicinal properties when properly stored. In some instances, manufacturers of
an approved drug product may apply to FDA to extend the product expiration date based on
available data.194 In some instances, and in response to drug shortages, FDA has approved
extensions of expiration dates for certain products.195
Provision
Section 2512 directs the HHS Secretary to issue or revise guidance related to expiration dates for
certain drug and biologic product applications. The guidance is to address (1) the submission of
stability data testing results in such applications with considerations for streamlining data
requirements to allow for faster review of longer expiration dates; (2) the labeling of a drug
product with the longest feasible expiration date supported by data; and (3) the use of innovative
approaches for product stability modelling. The Secretary must also submit a report to Congress
two years after enactment (and another two years later) that includes information on drug
products for which the HHS Secretary has requested the manufacturer to change the expiration
date and the circumstances of such requests.
Section 2513: Combating counterfeit devices.
Background
Leading up to and during the COVID-19 pandemic, there was concern about the import and
marketing of counterfeit medical products, especially counterfeit medical devices (e.g., COVID-
19 OTC tests).196 Although authorities addressing counterfeit drugs were in place prior to the
pandemic, similar authorities were not in place for medical devices. In early 2020, the
Safeguarding Therapeutics Act (H.R. 5663/S. 4225) was introduced to provide authority to the
FDA to destroy specified counterfeit medical devices refused admission into the United States
and to add a definition for the term “counterfeit device” in the FFDCA; this bill became law in
January 2021.197
Provision
Section 2513 amends FFDCA Section 301 to prohibit three actions related to counterfeit devices:

192 21 U.S.C. §360(i).
193 21 C.F.R. §211.137 and 21 C.F.R. §211.166.
194 FDA, “Changes to an Approved NDA or ANDA,” April 2004, p. 31, https://www.fda.gov/media/71846/download.
195 FDA, “Expiration Date Extension,” last updated April 27, 2023, https://www.fda.gov/emergency-preparedness-and-
response/mcm-legal-regulatory-and-policy-framework/expiration-dating-extension.
196 See, for example, FDA, “Counterfeit At-Home OTC COVID-19 Diagnostic Tests,” https://www.fda.gov/medical-
devices/coronavirus-covid-19-and-medical-devices/counterfeit-home-otc-covid-19-diagnostic-tests.
197 P.L. 116-304, amending §§801 and 201 of the FFDCA.
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(1) “forging, counterfeiting, simulating, falsely representing, or without proper authority
using any mark, stamp, tag, label, or other identification upon any device or container,
packaging, or labeling”;
(2) “making, selling, disposing of, or keeping in possession, control, or custody, or
concealing any punch, die, plate, stone, or other thing designed to print, imprint, or
reproduce the trademark, trade name, or other identifying mark or imprint of another or
any likeness of any of the foregoing upon any device or container, packaging, or labeling
thereof so as to render such device a counterfeit device”; and
(3) “the doing of any act which causes a device to be a counterfeit device, or the sale or
dispensing, or the holding for sale or dispensing, of a counterfeit device.”198
In addition, this provision amends FFDCA Section 303199 to create and clarify penalties for
certain of these prohibited acts.
Section 2514: Preventing medical device shortages
Background
As mandated by the CARES Act (P.L. 116-136), device manufacturers are required to report to
FDA during or prior to a public health emergency any permanent discontinuance of production,
or interruption in production, likely to lead to a significant disruption in the supply of a device,
including the reasons for the discontinuance or interruption.200 This information must be reported
to FDA at least six months prior to occurrence, or as soon as is practical.201 In contrast to the
agency’s authority to compel manufacturers of certain drugs to report discontinuances or
interruptions in production,202 FDA did not have such authority for medical devices prior to the
CARES Act. Rather, FDA relied on manufacturers to voluntarily report such information to the
agency.
FDA has issued guidance to help affected manufacturers implement this provision in the context
of COVID-19; this guidance expired when the public health emergency (PHE) ended.203 In
addition to outlining the requirements specified in statute, the guidance specified additional
voluntary information that would help the agency identify shortages.204 In January 2022, the
agency published draft guidance to elaborate on the requirements during any public health

198 21 U.S.C. §331.
199 21 U.S.C. §333.
200 FFDCA §506J(a); 21 U.S.C. §356j(a).
201 FFDCA §506J(b); 21 U.S.C. §356j(b). Per FDA guidance, FDA interprets “as soon as is practicable” to mean no
later than seven calendar days after the discontinuance or interruption in manufacturing occurs. FDA, Guidance for
Industry and Food and Drug Administration Staff: Notifying CDRH of a Permanent Discontinuance or Interruption in
Manufacturing of a Device Under Section 506J of the FD&C Act During the COVID-19 Public Health Emergency, p.
5, June 2020, https://www.fda.gov/media/137712/download (hereinafter FDA, Guidance: Notifying CDRH of a
Permanent Discontinuance or Interruption in Manufacturing of a Device Under Section 506J of the FD&C Act During
the COVID-19 Public Health Emergency).
202 21 U.S.C. §356c.
203 FDA, Guidance: Notifying CDRH of a Permanent Discontinuance or Interruption in Manufacturing of a Device
Under Section 506J of the FD&C Act During the COVID-19 Public Health Emergency.
204 FDA, Guidance: Notifying CDRH of a Permanent Discontinuance or Interruption in Manufacturing of a Device
Under Section 506J of the FD&C Act During the COVID-19 Public Health Emergency, November 2020, pp. 11-12,
https://www.fda.gov/media/137712/download.
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emergency, not only those that are COVID-specific.205 This broader guidance is in effect going
forward but notably continues to be in effect only during specified public health emergencies.
Provision
Section 2514 amends FFDCA Section 506J to allow FDA to receive voluntary notifications of
interruptions of or discontinuances in manufacture of certain devices, as specified, from device
manufacturers, including the reasons for such interruptions or discontinuances.206 The Secretary is
required, not later than one year after enactment, to publish draft guidance on these voluntary
notifications, including recommended timeframes and processes for the notifications, and
possible mitigating actions that the Secretary may take, among other things. The Secretary is
further required to publish final guidance not later than one year after the close of comments on
the draft guidance. In addition, the Secretary is required, not later than one year after enactment,
to issue or revise draft guidance on the device shortage notification requirements under Section
506J, including a list of device types for which shortage notifications are required.
Section 2515: Technical corrections
Section 2515 offers a number of technical corrections to various sections of the CARES Act and
the FFDCA.

Author Information

Kavya Sekar, Coordinator
Todd Kuiken
Analyst in Health Policy
Analyst in Science and Technology Policy

Hassan Z. Sheikh
Amanda K. Sarata
Analyst in Health Policy
Specialist in Health Policy

Johnathan H. Duff
Jared S. Sussman
Analyst in Health Policy
Analyst in Health Policy

Elayne J. Heisler
Nora Wells
Acting Section Research Manager
Analyst in Health Policy

205 FDA, Notifying FDA of a Permanent Discontinuance or Interruption in Manufacturing of a Device Under Section
506J of the FD&C Act, January 2022, https://www.fda.gov/media/155245/download.
206 21 U.S.C. §356c.
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Disclaimer
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under the direction of Congress. Information in a CRS Report should not be relied upon for purposes other
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copy or otherwise use copyrighted material.

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