H.R. 6133 · 117th Congress

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.

Stage
In committee
Sponsor
Ralph Norman
Introduced
2021-12-02
Latest action
2021-12-03 · Referred to the Subcommittee on Health.

Action history

  1. 2021-12-03Referred to the Subcommittee on Health.
  2. 2021-12-02Introduced in House
  3. 2021-12-02Referred to the House Committee on Energy and Commerce.