H.R.6433 - FDA User Fee Corrections Act of 2012
To make corrections with respect to Food and Drug Administration user fees. view all titles (4)
All Bill Titles
- Short: FDA User Fee Corrections Act of 2012 as enacted.
- Short: FDA User Fee Corrections Act of 2012 as passed senate.
- Short: FDA User Fee Corrections Act of 2012 as passed house.
- Official: To make corrections with respect to Food and Drug Administration user fees. as introduced.
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Official Summary
10/5/2012--Public Law. (This measure has not been amended since it was introduced. The summary of that version is repeated here.) FDA User Fee Corrections Act of 2012 - Amends the Federal Food, Drug, and Cosmetic Act (FFDCA), as amended by the Food and Drug Administration Safety and InnovaOfficial Summary
10/5/2012--Public Law. (This measure has not been amended since it was introduced. The summary of that version is repeated here.) FDA User Fee Corrections Act of 2012 - Amends the Federal Food, Drug, and Cosmetic Act (FFDCA), as amended by the Food and Drug Administration Safety and Innovation Act (P.L. 112-144), to:(1) make clerical corrections to provisions of such Act; and
(2) eliminate the restriction that appropriated funds shall be available only for payment of increases in the cost of reviewing medical device applications, including related personnel costs. Specifies due dates in FY2013 under FFDCA for the drug master file fee, the abbreviated new drug application and prior approval supplement filing fees, and the generic drug facility and active pharmaceutical ingredient facility fees.
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U.S. Congress - H.R.6433 FDA User Fee Corrections Act of 2012



