[Congressional Bills 119th Congress]
[From the U.S. Government Publishing Office]
[S. 5297 Introduced in Senate (IS)]
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119th CONGRESS
2d Session
S. 5297
To require the Administrator of the Centers for Medicare & Medicaid
Services to submit a report regarding the use of coverage and
reimbursement authorities to protect the markets for active
pharmaceutical ingredients and key staring materials.
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IN THE SENATE OF THE UNITED STATES
August 6, 2026
Mr. Schiff (for himself and Mr. Scott of Florida) introduced the
following bill; which was read twice and referred to the Committee on
Finance
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A BILL
To require the Administrator of the Centers for Medicare & Medicaid
Services to submit a report regarding the use of coverage and
reimbursement authorities to protect the markets for active
pharmaceutical ingredients and key staring materials.
Be it enacted by the Senate and House of Representatives of the
United States of America in Congress assembled,
SECTION 1. SHORT TITLE.
This Act may be cited as the ``American Pharmaceutical Security
Act''.
SEC. 2. REPORT ON MARKETS FOR API AND KEY STARTING MATERIALS.
(a) In General.--Not later than 1 year after the date of enactment
of this Act, the Administrator of the Centers for Medicare & Medicaid
Services (referred to in this section as the ``Administrator'') shall
submit to Congress a report on its findings and policy recommendations
regarding the use of coverage and reimbursement authorities to protect
the markets of the United States and its allies for active
pharmaceutical ingredients and key starting materials and reduce direct
and indirect dependence on foreign adversaries (as described in section
791.4 of title 15, Code of Federal Regulations (or any successor
regulations)) for such ingredients and materials.
(b) Contents.--The report under subsection (a)--
(1) may include--
(A) recommendations for price floor commitments in
support of domestic manufacturing of active
pharmaceutical ingredients and key starting materials
to protect investments in the domestic markets of such
ingredients and materials against nonmarket practices
and price manipulation; and
(B) recommendations that would prioritize
domestically manufactured active pharmaceutical
ingredients and key starting materials over foreign
manufactured active pharmaceutical ingredients and key
starting materials when a domestic source for the
applicable ingredient or material exists; and
(2) shall identify any existing gaps in data and
information related to the origin and ownership of active
pharmaceutical ingredients and key starting materials that the
Administrator would need to implement the recommendations
included in the report.
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