H.R.6433 - FDA User Fee Corrections Act of 2012112th Congress (2011-2012)
|Sponsor:||Rep. Upton, Fred [R-MI-6] (Introduced 09/19/2012)|
|Committees:||House - Energy and Commerce|
|Latest Action:||10/05/2012 Became Public Law No: 112-193. (TXT | PDF) (All Actions)|
This bill has the status Became Law
Here are the steps for Status of Legislation:
- Passed House
- Passed Senate
- To President
- Became Law
Summary: H.R.6433 — 112th Congress (2011-2012)All Information (Except Text)
Public Law No: 112-193 (10/05/2012)
(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.