HR 6133
117th Congress
House
Health
Cardiovascular and respiratory health
Drug safety, medical device, and laboratory regulation
Emergency medical services and trauma care
Government information and archives
Immunology and vaccination
Infectious and parasitic diseases
Licensing and registrations
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.
Introduced: December 2, 2021
Introduced by:
Norman, Ralph
Republican
· South Carolina
See on congress.gov
Everywhere this bill has been
3 steps
Introduced
In committee
Reported out
Passed House
Passed Senate
To President
Became law
Dec 3, 2021
Referred to the Subcommittee on Health.
Dec 2, 2021
Referred to the House Committee on Energy and Commerce.
Dec 2, 2021
Introduced in House
Plain-English 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.
What's happening now
Referred to the Subcommittee on Health.
Committees of jurisdiction
2