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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
Ralph Norman

Ralph Norman

Republican Representative

South Carolina

Cosponsors (20)
Diana Harshbarger (Republican)Bob Good (Republican)Paul A. Gosar (Republican)Chip Roy (Republican)Marjorie Taylor Greene (Republican)Scott Franklin (Republican)Jeff Duncan (Republican)Thomas Massie (Republican)Scott Perry (Republican)Barry Loudermilk (Republican)Pat Fallon (Republican)Dan Bishop (Republican)Daniel Webster (Republican)Michael Cloud (Republican)Madison Cawthorn (Republican)Mary E. Miller (Republican)Bill Posey (Republican)Randy K. Sr. Weber (Republican)Louie Gohmert (Republican)Brian Babin (Republican)

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
Dec 2, 2021
Introduced in House
Dec 2, 2021
Referred to the House Committee on Energy and Commerce.
Dec 3, 2021
Referred to the Subcommittee on Health.
  • December 2, 2021
    Introduced in House


  • December 2, 2021
    Referred to the House Committee on Energy and Commerce.


  • December 3, 2021
    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.
View Full Text

Suggested Questions

Get AI-generated questions to help you understand this bill better

Timeline
Dec 2, 2021
Introduced in House
Dec 2, 2021
Referred to the House Committee on Energy and Commerce.
Dec 3, 2021
Referred to the Subcommittee on Health.
  • December 2, 2021
    Introduced in House


  • December 2, 2021
    Referred to the House Committee on Energy and Commerce.


  • December 3, 2021
    Referred to the Subcommittee on Health.
Ralph Norman

Ralph Norman

Republican Representative

South Carolina

Cosponsors (20)
Diana Harshbarger (Republican)Bob Good (Republican)Paul A. Gosar (Republican)Chip Roy (Republican)Marjorie Taylor Greene (Republican)Scott Franklin (Republican)Jeff Duncan (Republican)Thomas Massie (Republican)Scott Perry (Republican)Barry Loudermilk (Republican)Pat Fallon (Republican)Dan Bishop (Republican)Daniel Webster (Republican)Michael Cloud (Republican)Madison Cawthorn (Republican)Mary E. Miller (Republican)Bill Posey (Republican)Randy K. Sr. Weber (Republican)Louie Gohmert (Republican)Brian Babin (Republican)

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