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.

United States117th CongressHR-6133House of Representatives
Updated: Dec 3, 2021

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.

Bill texts

Available versions
Introduced (House)View official text

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Timeline

  1. Referred to the House Committee on Energy and Commerce.

    House of Representatives

  2. Introduced in House

  3. Referred to the Subcommittee on Health.

    House of Representatives

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