Securing America’s Vaccines for Emergencies Act of 2022
A BILL
To amend the Defense Production Act of 1950 to ensure the supply of certain medical materials essential to national defense, and for other purposes.
Sec. 2 Securing essential medical materials
“(3) 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;”
“109. Strategy on securing supply chains for medical materials
“(a) In general—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 submit to the appropriate Members of Congress a strategy that includes the following:
“(1) 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.
“(2) An analysis of vulnerabilities to existing supply chains for such medical materials and recommendations to address the vulnerabilities.
“(3) Measures to be undertaken by the President to diversify such supply chains, as appropriate and as required for national defense.
“(4) A discussion of—
“(A) 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 in section 201 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 321));
“(B) 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; and
“(C) 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.
“(b) Progress Report—Not later than one year after submission of the strategy under subsection (a), and annually thereafter until September 30, 2025, the President shall submit to the appropriate Members of Congress a progress report—
“(1) evaluating the implementation of the strategy; and
“(2) including such updates to the strategy as the President considers appropriate.
“(c) Form of strategy and report—The strategy required by subsection (a) and the progress reports required by subsection (b) shall be submitted in unclassified form but may include a classified annex.
“(d) Appropriate Members of Congress—The term appropriate Members of Congress means—
“(1) the Speaker, majority leader, and minority leader of the House of Representatives;
“(2) the majority leader and minority leader of the Senate; and
“(3) the chairperson and ranking member of—
“(A) the Committee on Financial Services of the House of Representatives; and
“(B) the Committee on Banking, Housing, and Urban Affairs of the Senate.”
Sec. 3 Investment in supply chain security
“(h) Investment in supply chain security
“(1) In general—In addition to other authorities under 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.
“(2) Eligible entity—An eligible entity described in this paragraph is an entity that—
“(A) is organized under the laws of the United States or any jurisdiction within the United States; and
“(B) produces—
“(i) one or more critical components;
“(ii) critical technology; or
“(iii) one or more products or raw materials for the security of supply chains or supply chain activities.
“(3) Definitions—In this subsection, the terms supply chain and supply chain activities have the meanings given those terms by the President by regulation.”