Federal
United States Pharmaceutical Supply Chain Review Act
Source: Congress.gov ·
747 words in original text
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II
116TH CONGRESS
2D SESSION
S. 4191
To require a report on foreign investment in the pharmaceutical industry
of the United States.
IN THE SENATE OF THE UNITED STATES
JULY 2, 2020
Ms. WARREN introduced the following bill; which was read twice and referred
to the Committee on Banking, Housing, and Urban Affairs
A BILL
To require a report on foreign investment in the
pharmaceutical industry of the United States.
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 ‘‘United States Pharma-
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ceutical Supply Chain Review Act’’.
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SEC. 2. REPORT ON FOREIGN INVESTMENT IN PHARMA-
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CEUTICAL INDUSTRY.
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(a) IN GENERAL.—Not later than one year after the
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date of the enactment of this Act, and annually thereafter,
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the Federal Trade Commission, in consultation with the
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•S 4191 IS
Secretary of the Treasury acting through the Committee
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on Foreign Investment in the United States (in this sec-
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tion referred to as the ‘‘Committee’’), shall submit to the
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appropriate congressional committees, the Secretary of
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Health and Human Services, and the Commissioner of
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Food and Drugs, a report on foreign investment in the
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pharmaceutical industry of the United States.
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(b) ELEMENTS.—The report required by subsection
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(a) shall include the following:
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(1) An assessment of—
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(A) the supply chain of the pharmaceutical
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industry of the United States and the effect of
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concentration and reliance on foreign manufac-
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turing within that industry;
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(B) the effect of foreign investment in the
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pharmaceutical industry of the United States
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on domestic capacity to produce drugs and ac-
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tive and inactive ingredients of drugs; and
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(C) the effect of foreign investment in
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technologies or other products for sequencing or
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storage of DNA, including genome and exome
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analysis, in the United States, including the ef-
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fect of such investment on the capacity to se-
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quence or store DNA in the United States.
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•S 4191 IS
(2) The number of reviews and investigations
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conducted by the Committee, in each of the 10 fiscal
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years preceding the year in which the study is con-
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ducted, with respect to covered transactions (as de-
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fined in section 721(a) of the Defense Production
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Act of 1950 (50 U.S.C. 4565(a)))—
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(A) in the pharmaceutical industry of the
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United States; or
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(B) relating to the sequencing or storage
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of DNA in the United States.
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(3) A short description of each such review or
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investigation, including whether the transaction was
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approved or prohibited.
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(c) AUTHORITY.—The Federal Trade Commission
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shall have authority under section 6 of the Federal Trade
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Commission Act (15 U.S.C. 46) to conduct the studies re-
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quired to prepare the report required by subsection (a).
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(d) PUBLICATION.—The Federal Trade Commission
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shall publish an unclassified summary of the report re-
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quired by subsection (a) on a publicly available internet
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website of the Commission.
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(e) APPROPRIATE CONGRESSIONAL COMMITTEES DE-
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FINED.—In this section, the term ‘‘appropriate congres-
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sional committees’’ means—
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•S 4191 IS
(1) the Committee on Banking, Housing, and
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Urban Affairs, the Committee on Health, Education,
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Labor, and Pensions, the Committee on Armed
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Services, the Committee on Foreign Relations, the
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Committee on Commerce, Science, and Transpor-
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tation, and the Committee on Appropriations of the
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Senate; and
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(2) the Committee on Financial Services, the
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Committee on Energy and Commerce, the Com-
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mittee on Armed Services, the Committee on For-
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eign Affairs, and the Committee on Appropriations
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of the House of Representatives.
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Æ
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