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
Introduced
2021-12-02
Latest action
2021-12-03 · Referred to the Subcommittee on Health.

Subjects

Health
Infectious and parasitic diseases
Licensing and registrations
Emergency medical services and trauma care
Cardiovascular and respiratory health
Government information and archives
Immunology and vaccination
Drug safety, medical device, and laboratory regulation