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H.R. 6133

BillFederalHouseIn Committee
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.
About This Bill
Committee
Latest Action · December 3, 2021
Referred to the Subcommittee on Health.
Congress
117th (2021–2023)
Introduced
December 2, 2021
Cosponsors (20)
0D 20R
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Summary

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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.

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