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.
Health Subcommittee, Energy and Commerce Committee
Introduced
In Committee
On Floor
Passed Chamber
Enacted
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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Timeline
Introduced in House
Referred to the House Committee on Energy and Commerce.
Referred to the Subcommittee on Health.
Introduced in House
Referred to the House Committee on Energy and Commerce.
Referred to the Subcommittee on Health.
Health
Cardiovascular and respiratory healthDrug safety, medical device, and laboratory regulationEmergency medical services and trauma careGovernment information and archivesImmunology and vaccinationInfectious and parasitic diseasesLicensing and registrations
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.
USA117th CongressHR-6133| House
| Updated: 12/3/2021
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.
Health Subcommittee, Energy and Commerce Committee
Health
Introduced
In Committee
On Floor
Passed Chamber
Enacted
Cardiovascular and respiratory healthDrug safety, medical device, and laboratory regulationEmergency medical services and trauma careGovernment information and archivesImmunology and vaccinationInfectious and parasitic diseasesLicensing and registrations