Sec. 5121. SAVE Act of 2021
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Section 2(b) of the Defense Production Act of 1950 ( 50 U.S.C. 4502 ) is amended— by redesignating paragraphs
(3)through
(8)as paragraphs
(4)through (9), respectively; and by inserting after paragraph
(2)the following: authorities under this Act should be used when appropriate to ensure the availability of medical materials essential to national defense, including through measures designed to secure the drug supply chain, and taking into consideration the importance of United States competitiveness, scientific leadership and cooperation, and innovative capacity; . Section 107 of the Defense Production Act of 1950 ( 50 U.S.C. 4517 ) is amended— in subsection (a), by inserting (including medical materials) after materials ; and in subsection (b)(1), by inserting (including medical materials such as drugs, devices, and biological products to diagnose, cure, mitigate, treat, or prevent disease that are essential to national defense) after essential materials . Title I of the Defense Production Act of 1950 ( 50 U.S.C. 4511 et seq. ) is amended by adding at the end the following: Not later than 180 days after the date of the enactment of this section, the President, in consultation with the Secretary of Health and Human Services, the Secretary of Commerce, the Secretary of Homeland Security, and the Secretary of Defense, shall transmit a strategy to the appropriate Members of Congress that includes the following: A detailed plan to use the authorities under this title and title III, or any other provision of law, to ensure the supply of medical materials (including drugs, devices, and biological products (as that term is defined in section 351 of the Public Health Service Act ( 42 U.S.C. 262 )) to diagnose, cure, mitigate, treat, or prevent disease) essential to national defense, to the extent necessary for the purposes of this Act. An analysis of vulnerabilities to existing supply chains for such medical materials, and recommendations to address the vulnerabilities. Measures to be undertaken by the President to diversify such supply chains, as appropriate and as required for national defense. A discussion of— any significant effects resulting from the plan and measures described in this subsection on the production, cost, or distribution of biological products (as that term is defined in section 351 of the Public Health Service Act ( 42 U.S.C. 262 )) or any other devices or drugs (as defined under the Federal Food, Drug, and Cosmetic Act ( 21 U.S.C. 301 et seq. )); a timeline to ensure that essential components of the supply chain for medical materials are not under the exclusive control of a foreign government in a manner that the President determines could threaten the national defense of the United States; and efforts to mitigate any risks resulting from the plan and measures described in this subsection to United States competitiveness, scientific leadership, and innovative capacity, including efforts to cooperate and proactively engage with United States allies. Following submission of the strategy under subsection (a), the President shall submit to the appropriate Members of Congress an annual progress report until September 30, 2025, evaluating the implementation of the strategy, and may include updates to the strategy as appropriate. The strategy and progress reports shall be submitted in unclassified form but may contain a classified annex. The term appropriate Members of Congress means the Speaker, majority leader, and minority leader of the House of Representatives, the majority leader and minority leader of the Senate, the Chairman and Ranking Member of the Committee on Financial Services of the House of Representatives, and the Chairman and Ranking Member of the Committee on Banking, Housing, and Urban Affairs of the Senate. . Section 303 of the Defense Production Act of 1950 ( 50 U.S.C. 4533 ) is amended by adding at the end the following: In addition to other authorities in this title, the President may make available to an eligible entity described in paragraph
(2)payments to increase the security of supply chains and supply chain activities, if the President certifies to Congress not less than 30 days before making such a payment that the payment is critical to meet national defense requirements of the United States. An eligible entity described in this paragraph is an entity that— is organized under the laws of the United States or any jurisdiction within the United States; and produces— one or more critical components; critical technology; or one or more products or raw materials for the security of supply chains or supply chain activities. In this subsection, the terms supply chain and supply chain activities have the meanings given those terms by the President by regulation. . Not later than 90 days after the date of the enactment of this Act, the President shall prescribe regulations setting forth definitions for the terms supply chain and supply chain activities for the purposes of section 303(h) of the Defense Production Act of 1950 ( 50 U.S.C. 4533(h) ), as added by subsection (a). The definitions required by paragraph (1)— shall encompass— the organization, people, activities, information, and resources involved in the delivery and operation of a product or service used by the Government; or critical infrastructure as defined in Presidential Policy Directive 21 (February 12, 2013; relating to critical infrastructure security and resilience); and may include variations as determined necessary and appropriate by the President for purposes of national defense.
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