[Congressional Bills 119th Congress]
[From the U.S. Government Publishing Office]
[S. 5265 Introduced in Senate (IS)]

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119th CONGRESS
  2d Session
                                S. 5265

 To identify and take action against international trade practices of 
  high income countries that unfairly exploit innovation by deviating 
     from market-based policies and unfairly exploit United States 
                  innovation, and for other purposes.


_______________________________________________________________________


                   IN THE SENATE OF THE UNITED STATES

                             August 5, 2026

 Mr. Sheehy (for himself, Mr. McCormick, and Mr. Budd) introduced the 
 following bill; which was read twice and referred to the Committee on 
                                Finance

_______________________________________________________________________

                                 A BILL


 
 To identify and take action against international trade practices of 
  high income countries that unfairly exploit innovation by deviating 
     from market-based policies and unfairly exploit United States 
                  innovation, and for other purposes.

    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 ``Use Sovereignty To reduce Rx Act'' 
or the ``USTRx Act''.

SEC. 2. FINDINGS; SENSE OF CONGRESS.

    (a) Findings.--Congress finds the following:
            (1) Pharmaceutical price controls in foreign markets 
        distort global trade flows and competition by depressing the 
        prices of innovative drugs and exploiting pharmaceutical 
        innovations researched and developed in the United States.
            (2) By setting prices at levels that are not market-based, 
        such price controls undervalue the discovery of new, innovative 
        treatments, diminish opportunities and incentives for global 
        innovation in new medicines, and threaten to restrict access to 
        new treatments and cures for United States patients and 
        consumers.
            (3) Recognizing those dynamics, it is critical that the 
        United States use all available trade tools to address such 
        free-riding to ensure that foreign government regulatory 
        reimbursement regimes are transparent, provide procedural 
        fairness, are non-discriminatory, and provide full market 
        access to United States products.
    (b) Sense of Congress.--It is the sense of Congress that--
            (1) ensuring the security of innovative and affordable 
        healthcare is a top priority for the people of the United 
        States and for Congress;
            (2) foreign government policies that mandate artificially 
        low drug prices in foreign markets undermine that priority by 
        reducing global incentives to invest in the development of new 
        medicines;
            (3) such exploitative behavior unfairly shifts the cost of 
        developing new treatments to the United States and unduly 
        relies on United States patients and taxpayers to finance 
        global pharmaceutical innovation; and
            (4) safeguarding access to life-saving treatments for 
        United States patients requires combating such behavior so that 
        foreign countries pay their fair share of the costs associated 
        with the development of new drugs.

SEC. 3. CHIEF PHARMACEUTICAL TRADE NEGOTIATOR.

    Section 141 of the Trade Act of 1974 (19 U.S.C. 2171) is amended--
            (1) in subsection (b)(2)--
                    (A) in the first sentence, by inserting ``one Chief 
                Pharmaceutical Trade Negotiator,'' after ``one Chief 
                Agricultural Negotiator,''; and
                    (B) by inserting ``the Chief Pharmaceutical Trade 
                Negotiator,'' after ``the Chief Agricultural 
                Negotiator,'' each place it appears; and
            (2) in subsection (c), by adding at the end the following 
        new paragraph:
    ``(7) The principal functions of the Chief Pharmaceutical Trade 
Negotiator shall be to conduct trade negotiations, enforce trade 
agreements relating to United States pharmaceutical products, and take 
appropriate action to address acts, policies, or practices of high-
income countries that have a significant adverse impact on the ability 
of United States pharmaceutical manufacturers to enjoy full market 
access. The Chief Pharmaceutical Trade Negotiator shall be a vigorous 
advocate on behalf of United States manufacturers and consumers of 
pharmaceutical products and shall perform such other functions as the 
United States Trade Representative may direct. In carrying out such 
duties, the Chief Pharmaceutical Negotiator shall, as appropriate, 
consult or coordinate with the Chief Intellectual Property 
Negotiator.''.

SEC. 4. ANNUAL REPORT ON ACTS, POLICIES, AND PRACTICES OF HIGH INCOME 
              COUNTRIES.

    (a) List of High Income Countries.--The United States Trade 
Representative shall compile and annually update a list of each foreign 
country that is defined as ``high income'' by the official statistics 
of the International Bank for Reconstruction and Development of the 
World Bank.
    (b) Report Required.--With respect to each country included on the 
most recent list required under subsection (a), the United States Trade 
Representative, acting through the Chief Pharmaceutical Trade 
Negotiator (as established pursuant to the amendments made by section 
3), shall annually submit to the Committee on Ways and Means of the 
House of Representatives and the Committee on Finance of the Senate and 
concurrently publish on a publicly available website of the United 
States Trade Representative a report that--
            (1) describes in detail the results of a review of the 
        acts, policies, and practices of such country relating to the 
        trade in pharmaceutical products in the previous fiscal year;
            (2) determines whether such acts, policies, or practices--
                    (A) are not developed and implemented in a fair, 
                nondiscriminatory, and transparent manner;
                    (B) are not market-based or do not appropriately 
                recognize the value of innovative medicines;
                    (C) deny reciprocal market access for United States 
                products;
                    (D) diminish incentives for innovation in a manner 
                that delays, prevents, or otherwise adversely impacts 
                the introduction of new medicines in the United States;
                    (E) violate or are inconsistent with the provisions 
                of, or otherwise deny benefits to the United States 
                under, any bilateral or multilateral trade agreement 
                with such country; and
                    (F) are unjustifiable or impose a significant 
                burden or unreasonable or discriminatory restriction on 
                United States commerce with such country; and
            (3) describes the current status of any responsive actions 
        taken by the United States with respect to acts, policies, or 
        practices for which the United States Trade Representative has 
        determined and included in any prior report, pursuant to 
        paragraph (2), that the interests of the United States are 
        harmed, including responsive actions pursuant to title III of 
        the Trade Act of 1974 (19 U.S.C. 2411 et seq.).

SEC. 5. RESPONSE TO ADVERSE ACTIONS BY HIGH INCOME COUNTRIES.

    Not later than 30 days after the United States Trade Representative 
determines that an act, policy, or practice of a country included in 
the most recent list required under section 4(a) meets any of the 
criteria described in section 4(b)(2), the United States Trade 
Representative shall submit to Committee on Ways and Means of the House 
of Representatives and the Committee on Finance of the Senate a plan to 
respond to the act, policy, or practice, which may include initiating 
an investigation under title III of the Trade Act of 1974 (19 U.S.C. 
2411 et seq.), in accordance with section 302(b)(1) of that Act.
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