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

Bill Text Versions

1

Introduced in House

Published: December 2, 2021

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