Food and Drug Administration Safety and Innovation Act
Official title: “To amend the Federal Food, Drug, and Cosmetic Act to revise and extend the user-fee programs for prescription drugs and medical devices, to establish user-fee programs for generic drugs and biosimilars, and for other purposes.”
What this law changes
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Transparency Score
The Transparency Score is the share of this law’s dollars that goes to what the law says it is for. We have not read this law for this section yet.
Press releases by members of Congress
No saved press release names this law.
Read from 539 of 539 members' sites, releases since January 3, 2025, through October 7, 2026.
Press releases by organizations
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Read from 510 of 510 organizations' sites, releases since January 3, 2025, through October 7, 2026.
How it passed
The House passed it by voice vote on June 20, 2012. A voice vote records no individual votes.
The Senate passed it 92 to 4 on June 26, 2012, with 4 senators who did not vote.
It became law on July 9, 2012.
The question on the official record: Senate, “On the Motion (Motion to Concur in the House Amendment to Accompany S. 3187)”.
| Chamber and party | Yes | No | Present | Did not vote |
|---|---|---|---|---|
| Senate Republicans | 41 | 3 | 0 | 3 |
| Senate Democrats | 50 | 0 | 0 | 1 |
| Senate independents | 1 | 1 | 0 | 0 |
How each member voted
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Where this comes from
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