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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. 9/27/2007--Public Law.    (There is 1 other summary) (This measure has not been amended since it was introduced. The summary has been expanded because action occurred on the measure.)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 [...]

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Latest Actions
  • 09/27/2007 - Signed by President.
  • 09/27/2007 - Became Public Law No: 110-85.
  • 09/26/2007 - Presented to President.
  • 09/21/2007 - Message on Senate action sent to the House.
  • 09/20/2007 - Cleared for White House.

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Bill Text
File name Last Updated
H.R.3580 Received in Senate from House09/28/2007
H.R.3580 Enrolled as Agreed to or Passed by Both House and Senate09/28/2007
H.R.3580 Considered and Passed by House09/23/2007
H.R.3580 Engrossed as Agreed to or Passed by House09/21/2007