[Congressional Bills 119th Congress]
[From the U.S. Government Publishing Office]
[S. 5316 Introduced in Senate (IS)]

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119th CONGRESS
  2d Session
                                S. 5316

 To amend title VIII of the Defense Production Act of 1950 to include 
   biotechnology in the definitions of ``prohibited technology'' and 
           ``notifiable technology'', and for other purposes.


_______________________________________________________________________


                   IN THE SENATE OF THE UNITED STATES

                             August 6, 2026

  Mr. Ricketts (for himself and Ms. Slotkin) introduced the following 
 bill; which was read twice and referred to the Committee on Banking, 
                       Housing, and Urban Affairs

_______________________________________________________________________

                                 A BILL


 
 To amend title VIII of the Defense Production Act of 1950 to include 
   biotechnology in the definitions of ``prohibited technology'' and 
           ``notifiable technology'', 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 ``Biotech Investment National Security 
Act of 2026'' or the ``BINSA Act''.

SEC. 2. FINDINGS; SENSE OF CONGRESS.

    (a) Findings.--Congress finds the following:
            (1) The People's Republic of China has pursued a 
        deliberate, state-directed strategy to dominate global 
        biotechnology, including pharmaceutical development, biologics 
        manufacturing, and clinical research and development 
        capabilities.
            (2) United States capital flowing to Chinese biotechnology 
        companies through licensing agreements, joint ventures, and 
        equity investments is accelerating the acquisition by the 
        People's Republic of China of pharmaceutical intellectual 
        property and clinical development capabilities in a manner that 
        creates strategic dependency risks for the United States.
            (3) Cross-border out-licensing transactions between United 
        States and European pharmaceutical companies and Chinese 
        biotechnology firms totaled approximately $136,000,000,000 in 
        2025, representing a rapid and accelerating transfer of 
        pharmaceutical innovation capacity to entities subject to the 
        direction and control of the People's Republic of China.
            (4) Biotechnology, including pharmaceutical development and 
        biologics manufacturing, has civil-military dual-use 
        applications and presents strategic dependency risks for the 
        United States comparable to those presented by semiconductors, 
        artificial intelligence, and other technologies already covered 
        by title VIII of the Defense Production Act of 1950 (50 U.S.C. 
        4581 et seq.).
            (5) Section 851 of the National Defense Authorization Act 
        for Fiscal Year 2026 (Public Law 119-60; 41 U.S.C. 3901 note 
        prec.) (commonly referred to as the ``BIOSECURE Act''), 
        recognized that biotechnology is both a national security asset 
        and a strategic vulnerability, and that the People's Republic 
        of China seeks to dominate biotechnology as an industry of the 
        future.
    (b) Sense of Congress.--It is the sense of Congress that consistent 
application of outbound investment screening to biotechnology is 
necessary to prevent United States capital and intellectual property 
from accelerating the dominance by the People's Republic of China of 
the pharmaceutical innovation supply chain in a manner that will create 
long-term strategic dependency risks analogous to those the United 
States now faces with respect to rare earth elements and 
semiconductors.

SEC. 3. INCLUSION OF BIOTECHNOLOGY AND LICENSING OF TECHNOLOGIES IN 
              PROHIBITED AND NOTIFIABLE TRANSACTIONS.

    Section 809 of the Defense Production Act of 1950 (50 U.S.C. 4589) 
is amended--
            (1) in paragraph (4)(A)--
                    (A) in clause (vii), by striking ``; or'' and 
                inserting a semicolon;
                    (B) by redesignating clause (viii) as clause (ix); 
                and
                    (C) by inserting after clause (viii) the following:
                            ``(viii) licensing of a prohibited 
                        technology from a covered foreign person; or'';
            (2) in paragraph (7)(A), by adding at the end the 
        following:
                            ``(vi) Biotechnology, meaning the research, 
                        development, manufacturing, or 
                        commercialization of--
                                    ``(I) pharmaceutical products 
                                (which has the meaning given the term 
                                `drug' in section 201(g)(1) of the 
                                Federal Food, Drug, and Cosmetic Act 
                                (21 U.S.C. 321(g)(1)));
                                    ``(II) biological products (as 
                                defined in section 351(i) of the Public 
                                Health Service Act (42 U.S.C. 262(i))); 
                                and
                                    ``(III) therapeutic compounds, 
                                including drug discovery platforms, 
                                clinical research and development 
                                capabilities, biologics manufacturing, 
                                and intellectual property and know-how 
                                relating to therapeutic compounds.''; 
                                and
            (3) in paragraph (10)(A), by adding at the end the 
        following:
                            ``(vi) Biotechnology, meaning the research, 
                        development, manufacturing, or 
                        commercialization of--
                                    ``(I) pharmaceutical products 
                                (which has the meaning given the term 
                                `drug' in section 201(g)(1) of the 
                                Federal Food, Drug, and Cosmetic Act 
                                (21 U.S.C. 321(g)(1)));
                                    ``(II) biological products (as 
                                defined in section 351(i) of the Public 
                                Health Service Act (42 U.S.C. 262(i))); 
                                and
                                    ``(III) therapeutic compounds, 
                                including drug discovery platforms, 
                                clinical research and development 
                                capabilities, biologics manufacturing, 
                                and intellectual property and know-how 
                                relating to therapeutic compounds.''.

SEC. 4. RULEMAKING.

    (a) In General.--The Secretary of the Treasury shall, not later 
than 1 year after the date of the enactment of this Act, issue a rule 
to further define the parameters of the area of ``biotechnology'', as 
used in paragraphs (7)(A) and (10)(A) of section 809 of the Defense 
Production Act of 1950, as amended by section 3.
    (b) Requirements.--When defining the parameters of the area of 
``biotechnology'' pursuant to subsection (a), the Secretary of the 
Treasury shall--
            (1) consult with the Secretary of Health and Human 
        Services, the Secretary of Defense, and the Director of 
        National Intelligence;
            (2) give particular consideration to transactions involving 
        the licensing of intellectual property, drug discovery 
        platforms, clinical research and development capabilities, and 
        biologics manufacturing know-how to covered foreign persons (as 
        defined in section 809 of the Defense Production Act of 1950);
            (3) give particular consideration to licensing 
        transactions, joint ventures, and equity investments involving 
        drug discovery platforms, clinical development capabilities, 
        and biologics manufacturing as priority categories for both the 
        prohibited and notifiable technology tiers within the 
        biotechnology sector;
            (4) consider the degree to which a transaction would 
        transfer pharmaceutical innovation capacity, clinical 
        development capabilities, or manufacturing know-how to entities 
        subject to the direction or control of the People's Republic of 
        China; and
            (5) not define the biotechnology sector in a manner that 
        includes or could be construed to include agricultural 
        biotechnology, industrial fermentation unrelated to 
        pharmaceutical or therapeutic production, or basic academic 
        research with no direct pharmaceutical or therapeutic 
        application.

SEC. 5. REPORT REQUIRED.

    (a) In General.--Not later than 60 days after the date of the 
enactment of this Act, the Secretary of Defense shall submit to the 
appropriate congressional committees a report assessing whether flows 
of the United States capital into the biotechnology sector of the 
People's Republic of China, including through licensing transactions 
with Chinese biotechnology firms, negatively affect the United States 
national security and military readiness.
    (b) Form.--The report required by subsection (a) shall be submitted 
in unclassified form but may include a classified annex.
    (c) Appropriate Congressional Committees Defined.--In this section, 
the term ``appropriate congressional committees'' means--
            (1) the Committee on Armed Services of the House of 
        Representatives;
            (2) the Committee on Financial Services of the House of 
        Representatives;
            (3) the Permanent Select Committee on Intelligence of the 
        House of Representatives;
            (4) the Select Committee on the Strategic Competition 
        between the United States and the Chinese Communist Party of 
        the House of Representatives;
            (5) the Committee on Armed Services of the Senate;
            (6) the Committee on Banking, Housing, and Urban Affairs of 
        the Senate; and
            (7) the Select Committee on Intelligence of the Senate.
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