Federal
Taxpayer Research and Coronavirus Knowledge Act of 2020
Source: Congress.gov ·
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II
116TH CONGRESS
2D SESSION
S. 4539
To direct the Secretary of Health and Human Services and other Federal
officials to compile into a searchable database information relating to
Federal support for biomedical research and development related to
COVID–19, and for other purposes.
IN THE SENATE OF THE UNITED STATES
SEPTEMBER 8, 2020
Mr. MERKLEY (for himself and Mr. BRAUN) introduced the following bill;
which was read twice and referred to the Committee on Health, Edu-
cation, Labor, and Pensions
A BILL
To direct the Secretary of Health and Human Services and
other Federal officials to compile into a searchable data-
base information relating to Federal support for bio-
medical research and development related to COVID–
19, and for other purposes.
Be it enacted by the Senate and House of Representa-
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tives of the United States of America in Congress assembled,
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SECTION 1. SHORT TITLE.
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This Act may be cited as the ‘‘Taxpayer Research
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and Coronavirus Knowledge Act of 2020’’.
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•S 4539 IS
SEC. 2. DATABASE.
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(a) IN GENERAL.—The Secretary of Health and
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Human Services, the Director of the National Institutes
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of Health, the Assistant Secretary for Preparedness and
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Response, the Director of the Biomedical Advanced Re-
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search and Development Authority, the Secretary of De-
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fense, the Secretary of Veterans Affairs, the Director of
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the National Institute of Allergy and Infectious Diseases,
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and such other Federal officials as the Secretary of Health
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and Human Services determines to be appropriate, acting
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in coordination, shall—
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(1) compile into a searchable database informa-
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tion relating to Federal support (before or after the
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date of enactment of this Act) for biomedical re-
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search and development related to COVID–19 (in-
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cluding biomedical research and development relat-
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ing to a product or therapy that was later modified
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or repurposed to be used for COVID–19); and
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(2) make such database available on the public
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website of the Department of Health and Human
20
Services.
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(b) COVERED INFORMATION.—The information relat-
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ing to Federal support referred to in subsection (a)(1) in-
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cludes all contracts, funding agreements, licensing ar-
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rangements, other transactions, and other arrangements
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entered into by the Federal Government and tax benefits
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•S 4539 IS
provided with respect to research and development, and
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manufacturing, of a drug (including biological products),
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cell or gene therapy, or medical device intended to be man-
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ufactured,
used,
designed,
developed,
modified,
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repurposed, licensed, or procured to diagnose, mitigate,
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prevent, treat, or cure COVID–19, including the following:
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(1) Licensing agreements pursuant to section
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207 of title 35, United States Code.
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(2) Cooperative research and development
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agreements and licensing agreements pursuant to
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section 12 of the Stevenson-Wydler Technology In-
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novation Act of 1980 (15 U.S.C. 3710a).
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(3) Funding agreements, as defined in section
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201 of title 35, United States Code.
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(4) Other transactions entered into pursuant to
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the following:
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(A) Section 319L of the Public Health
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Service Act (42 U.S.C. 247d–7e).
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(B) Section 105 of the National Institutes
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of Health Reform Act of 2006 (42 U.S.C.
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284n).
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(C) Section 480 of the Public Health Serv-
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ice Act (42 U.S.C. 287a).
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(D) Section 421 of the Public Health Serv-
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ice Act (42 U.S.C. 285b–3).
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(E) Section 2371 of title 10, United States
1
Code.
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(5) Tax credits and deductions associated
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with—
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(A) qualified clinical testing expenses, as
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defined in section 45C of the Internal Revenue
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Code of 1986;
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(B) qualified research expenses, as defined
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in section 41 of the Internal Revenue Code of
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1986; and
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(C) charitable contributions, as defined in
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section 170(c) of the Internal Revenue Code of
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1986, to patient assistance programs.
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(c) INFORMATION REQUIRED.—Notwithstanding any
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other provision of law, the Federal officials referred to in
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subsection (a) shall include in the database under sub-
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section (a), with regard to each contract, funding agree-
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ment, licensing arrangement, other transaction, other ar-
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rangement, or tax benefit described in subsection (b), at
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least the following information:
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(1) The agency, program, institute, or other
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Federal Government entity providing the Federal
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support.
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(2) The amount and period of Federal financial
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support with an itemized breakdown.
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(3) Other Federal nonfinancial support, includ-
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ing the use of Federal personnel, Federal facilities,
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and Federal equipment.
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(4) The grant number, if applicable.
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(5) Associated clinical trial data, upon trial
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completion.
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(6) Associated patents and patent applications,
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specifying—
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(A) any Federal ownership in such patents
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and patent applications;
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(B) the expiration date of such patents
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and filing dates of such patent applications; and
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(C) the numbers of such patents and pat-
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ent applications.
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(7) Associated periods of marketing exclusivity
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under Federal law and the durations of such peri-
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ods.
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(8) The corporation, nonprofit organization,
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academic institution, person, or other entity receiv-
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ing the Federal support.
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(9) Any products (including repurposed prod-
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ucts) approved, authorized, or cleared for marketing,
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or for which marketing approval, authorization, or
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clearance is being sought, the development of which
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was aided by Federal support, including—
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(A) the names of such products;
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(B) the prices of such products; and
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(C) the current and anticipated manufac-
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turing capacity to produce such products.
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(10) The full terms of the contract, funding
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agreement, licensing arrangement, other transaction,
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or other arrangement described in subsection (b).
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(d) FORMAT OF INFORMATION.—The database under
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subsection (a) shall be—
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(1) searchable and filterable according to the
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categories of information described in subsection (c);
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and
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(2) presented in a user-friendly format.
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(e) TIMING.—The database under subsection (a)
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shall be—
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(1) made publicly available not later than 1
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month of the date of enactment of this Act; and
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(2) updated not less than every 30 days.
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(f) DISCLOSURE.—
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(1) IN GENERAL.—Notwithstanding any other
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provision of law, to the extent necessary for an offi-
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cial referred to in subsection (a) to carry out this
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section, such official may require entities receiving
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Federal support referred to in subsection (a)(1) to
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disclose to the official any information relating to
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such Federal support and required to be included in
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the database under subsection (a).
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(2) PENALTY FOR NONDISCLOSURE.—If an en-
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tity that is required to disclose information pursuant
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to paragraph (1) fails to disclose such information
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within a reasonable period of time or within 2 weeks
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of the official requesting such information, whichever
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is sooner, then such entity and all executive officers
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employed by such entity shall no longer be eligible
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for the receipt of Federal support in the form of a
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contract, funding agreement, licensing arrangement,
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other transaction, or other arrangement.
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Æ
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