[Congressional Bills 117th Congress]
[From the U.S. Government Publishing Office]
[H.R. 6133 Introduced in House (IH)]

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117th CONGRESS
  1st Session
                                H. R. 6133

  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.


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                    IN THE HOUSE OF REPRESENTATIVES

                            December 2, 2021

 Mr. Norman (for himself, Mr. Massie, Mr. Duncan, Mr. Perry, Mr. Roy, 
Mr. Good of Virginia, Mr. Webster of Florida, Mrs. Miller of Illinois, 
   Mr. Weber of Texas, Mr. Cawthorn, Mr. Posey, Mr. Bishop of North 
    Carolina, Mr. Gohmert, Mr. Gosar, Mr. Babin, and Mrs. Greene of 
   Georgia) introduced the following bill; which was referred to the 
                    Committee on Energy and Commerce

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                                 A BILL


 
  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.

    Be it enacted by the Senate and House of Representatives of the 
United States of America in Congress assembled,

SECTION 1. PUBLIC DISCLOSURE OF INFORMATION SUBMITTED TO FDA FOR 
              AUTHORIZING EMERGENCY USE OF, OR LICENSING, ANY COVID-19 
              VACCINE.

    Not later than 100 days after the date of enactment of this Act, 
the Commissioner of Food and Drugs shall 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.
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