Bill

Bill > HR6133


US HR6133

US HR6133
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.


summary

Introduced
12/02/2021
In Committee
12/03/2021
Crossed Over
Passed
Dead
01/03/2023

Introduced Session

117th Congress

Bill Summary

A BILL 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 con- junction with authorizing the emergency use of, or licens- ing, a COVID-19 vaccine.

AI Summary

This bill requires the Commissioner of the Food and Drug Administration (FDA) to make publicly available all records of information submitted to the FDA for the purpose of authorizing the emergency use of or licensing any COVID-19 vaccine. This includes any data or documents submitted to the FDA as part of the process for approving or authorizing the use of COVID-19 vaccines. The bill mandates that the Commissioner make these records publicly accessible within 100 days of the bill's enactment.

Committee Categories

Business and Industry, Health and Social Services

Sponsors (21)

Last Action

Referred to the Subcommittee on Health. (on 12/03/2021)

bill text


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