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Food and Drug Administration Safety and Innovation Act
Author(s): Senate and House of Representatives of the United States of America in Congress assembled (Author)
- Publisher: The United States Government
- Publication Date: 3 Jan. 2012
- Language: English
- Print length: 188 pages
- ISBN-10: B008YK5GY8
Book Description
An Act 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.
‘‘Prescription Drug User Fee Amendments of 2012’’.
‘‘Medical Device User Fee Amendments of 2012’’.
‘‘Generic Drug User Fee Amendments of 2012’’.
‘‘Biosimilar User Fee Act of 2012’’.
