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United States · Bill · HR

H.R. 6377 (117th)

Free At-Home Tests for All Act

referredUnited States· United States Congress· EN

Introduced

12 January 2022

Last action

13 January 2022 · Referred

Status

Referred to the Subcommittee on Health.

Sponsors

Rep. Beyer, Donald S. [D-VA-8], Rep. Titus, Dina [D-NV-1], Rep. Morelle, Joseph D. [D-NY-25], Kaiali'i Kahele, Rep. Ruiz, Raul [D-CA-25], Del. Norton, Eleanor Holmes [D-DC-At Large], Rep. Moore, Gwen [D-WI-4], Rep. Bishop, Sanford D. [D-GA-2], Rep. Peters, Scott H. [D-CA-50], Rep. Dean, Madeleine [D-PA-4], Rep. Blumenauer, Earl [D-OR-3], Rep. DeSaulnier, Mark [D-CA-10]

Subjects

Healthcare, Defence

Source updated

3 January 2025

Healthcare · Defence

Summary

Free At-Home Tests for All Act This bill requires the Department of Health and Human Services (HHS) to provide free antigen diagnostic tests for COVID-19 (i.e., rapid tests) to U.S. residents. The bill also automatically grants emergency use authorization for rapid tests approved by certain foreign regulators. Specifically, HHS must purchase a sufficient quantity of rapid tests to provide two tests per week at no cost to each resident for the 12 months following the bill's enactment. The President may use authorities available under the Defense Production Act of 1950 to obtain the tests. That act confers upon the President a broad set of authorities to influence domestic industry in order to provide essential materials and goods needed for the national defense. In addition, HHS must conduct outreach about the availability of free rapid tests to Medicare and Medicaid participants and make the tests available through those programs. The bill also automatically grants emergency use authorization during the public health emergency for rapid tests that are listed for emergency use by (1) the World Health Organization (WHO), or (2) a foreign regulator that is a stringent regulatory authority as defined by the WHO for purposes of medicine procurement. The Food and Drug Administration (FDA) may rescind authority for, or otherwise regulate, a rapid test that was automatically authorized. Additionally, the FDA must establish a permanent advisory committee focused on diagnostic and serological testing for public health needs.

This text is taken from the official record. PoliticalRepo does not editorialize.

Timeline

  1. 12 January 2022

    Introduced

    Referred to the Committee on Energy and Commerce, and in addition to the Committees on Financial Services, and Ways and Means, for a period to be subsequently determined by the Speaker, in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned.

    Source: IntroReferral

  2. 12 January 2022

    Introduced

    Introduced in House

    Source: IntroReferral

  3. 12 January 2022

    Introduced

    Introduced in House

    Source: IntroReferral

  4. 12 January 2022

    Referred

    Referred to the Subcommittee on Health.

    Source: Committee

  5. 13 January 2022

    Referred

    Referred to the Subcommittee on Health.

    Source: Committee

Votes

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Versions

Documents

3 official files

Introduced in House (text)

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  • Introduced in House (text)

    Introduced in House · EN · 12 January 2022

    ViewDownloadOpen at official source

  • Introduced in House (PDF)

    Introduced in House · EN · 12 January 2022

    ViewDownloadOpen at official source

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  • Introduced in House

    summary · EN · 12 January 2022

    Open at official source

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Sponsors

Related records

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Sources

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