H.R. 6133 · 117th Congress · House

To require the Commissioner of Food and Drugs to make available for public inspection all records of information submitted to the Food and Drug Administration in conjunction with authorizing the emergency use of, or licensing, a COVID-19 vaccine.

Active· Referred to the Subcommittee on Health.
Introduced
Dec 2, 21
Passed House
Pending
Passed Senate
Pending
Sent to President
Pending
Signed into Law
Pending

Executive Summary

This bill requires the Food and Drug Administration (FDA) to make publicly available all records of information submitted to the FDA in conjunction with the emergency use authorization or licensing of a COVID-19 vaccine.

Action Timeline

4
  1. DEC 03, 2021•Committee

    Referred to the Subcommittee on Health.

  2. DEC 02, 2021•IntroReferral

    Introduced in House

  3. DEC 02, 2021•IntroReferral

    Introduced in House

  4. DEC 02, 2021•IntroReferral

    Referred to the House Committee on Energy and Commerce.

Committees

2

Health Subcommittee

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Referred: Dec 3, 2021

Active

Energy and Commerce Committee

hsif00

Referred: Dec 2, 2021

Active