H.R.3580 - Federal Government

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.  

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  • Signed by President.
    09/27/2007
  • Became Public Law No: 110-85.
    09/27/2007
  • Presented to President.
    09/26/2007
  • Message on Senate action sent to the House.
    09/21/2007
  • Passed Senate without amendment by Unanimous Consent. (consideration: CR S11831-11841)
    09/20/2007
  • Cleared for White House.
    09/20/2007
  • Referred to the House Committee on Energy and Commerce.
    09/19/2007
  • Mr. Dingell moved to suspend the rules and pass the bill.
    09/19/2007
  • Considered under suspension of the rules. (consideration: CR H10551-10599)
    09/19/2007
  • On motion to suspend the rules and pass the bill Agreed to by the Yeas and Nays: (2/3 required): 405 - 7 (Roll no. 885). (text: CR H10551-10594)
    09/19/2007
  • Motion to reconsider laid on the table Agreed to without objection.
    09/19/2007
  • Received in the Senate.
    09/19/2007
  • Received in the Senate, read twice.
    09/19/2007
  • DEBATE - The House proceeded with forty minutes of debate on H.R. 3580.
    09/19/2007
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10/11/2009
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