H.R. 6133 · 117th Congress

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.

Stage
In committee
Introduced
2021-12-02
Latest action
2021-12-03 · Referred to the Subcommittee on Health.

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.