US SB297 | 2017-2018 | 115th Congress
Status
Spectrum: Slight Partisan Bill (Democrat 2-1)
Status: Introduced on February 2 2017 - 25% progression, died in committee
Action: 2017-02-02 - Read twice and referred to the Committee on Health, Education, Labor, and Pensions.
Pending: Senate Health, Education, Labor, And Pensions Committee
Text: Latest bill text (Introduced) [PDF]
Status: Introduced on February 2 2017 - 25% progression, died in committee
Action: 2017-02-02 - Read twice and referred to the Committee on Health, Education, Labor, and Pensions.
Pending: Senate Health, Education, Labor, And Pensions Committee
Text: Latest bill text (Introduced) [PDF]
Summary
Increasing Competition in Pharmaceuticals Act This bill amends the Federal Food, Drug, and Cosmetic Act to revise provisions regarding review and approval of generic drug applications or supplements to generic drug applications for drugs: (1) for which there is a shortage, or (2) that have not been recently introduced to the market by more than one manufacturer and for which tentative approval has not been granted to more than two applications. The Food and Drug Administration (FDA) must prioritize the review of such submissions and act on them within 150 days. User fees are waived for such an application unless the drug is under patent. The FDA may expedite the inspection of a facility proposed to manufacture such a drug. The FDA must award a transferrable generic drug priority review voucher to the sponsor of such an application upon approval. A voucher may be used to have the FDA review and take action upon a generic drug application within 150 days of submission. The FDA may revoke a voucher awarded for a drug that is not marketed within one year of approval. This voucher program is terminated at the end of FY2022. The FDA must periodically report on generic drug applications filed before FY2016 that are still pending. For a new drug application to be eligible for a priority review voucher as a tropical disease product application, the application must include new, essential clinical investigations. The Government Accountability Office must study the FDA's program for drug risk evaluation and mitigation strategies.
Title
Increasing Competition in Pharmaceuticals Act
Sponsors
Sen. Susan Collins [R-ME] | Sen. Claire McCaskill [D-MO] | Sen. Jon Tester [D-MT] |
History
Date | Chamber | Action |
---|---|---|
2017-02-02 | Senate | Read twice and referred to the Committee on Health, Education, Labor, and Pensions. |
Same As/Similar To
HB749 (Related) 2017-02-03 - Referred to the Subcommittee on Health.
Subjects
Congressional oversight
Drug safety, medical device, and laboratory regulation
Drug trafficking and controlled substances
Government studies and investigations
Health
Infectious and parasitic diseases
Licensing and registrations
Prescription drugs
User charges and fees
Drug safety, medical device, and laboratory regulation
Drug trafficking and controlled substances
Government studies and investigations
Health
Infectious and parasitic diseases
Licensing and registrations
Prescription drugs
User charges and fees
US Congress State Sources
Type | Source |
---|---|
Summary | https://www.congress.gov/bill/115th-congress/senate-bill/297/all-info |
Text | https://www.congress.gov/115/bills/s297/BILLS-115s297is.pdf |