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Latest Update: Wednesday, July, 09th 2008

To amend the Federal Food, Drug, and Cosmetic Act to revise and extend the user-fee programs for prescription drugs and for medical devices, to enhance the postmarket authorities of the Food and Drug Administration with respect to the safety of drugs, and for other purposes. 7/11/2007--Passed House amended.    (There is 1 other summary) Food and Drug Administration Amendments Act of 2007 - Title I: Prescription Drug User Fee Amendments of 2007 - (Sec. 101) Prescription Drug User Fee Amendments of 2007 - (Sec. 102) Amends the Federal Food, Drug, and Cosmetic Act (FFDCA) to include postmarket safety activities within the process for the review of human drug applications or supplements, including: (1) developing and using improved adverse event data collection systems and improved analytical tools to assess potential safety problems; (2) implementing and enforcing provisions relating to postapproval studies, clinical trials, labeling changes, and risk [...]

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Latest Actions
  • 07/16/2007 - Received in the Senate. Read twice. Placed on Senate Legislative Calendar under General Orders. Calendar No. 270.
  • 07/11/2007 - Reported by the Committee on Energy and Commerce. H. Rept. 110-225.
  • 07/11/2007 - Placed on the Union Calendar, Calendar No. 140.
  • 07/11/2007 - Mr. Dingell moved to suspend the rules and pass the bill, as amended.
  • 07/11/2007 - Considered under suspension of the rules. (consideration: CR H7568-7606)

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Bill Text
File name Last Updated
H.R.2900 Placed on Calendar in Senate08/31/2007
H.R.2900 Reported in House08/31/2007
H.R.2900 Engrossed as Agreed to or Passed by House08/31/2007
H.R.2900 Introduced in House08/31/2007