U.S. Congress - Drug safety, medical device, and laboratory regulation 
Issue: Drug safety, medical device, and laboratory regulation
Issue's Views
- Today: 12
- Past Seven Days: 26
- All-Time: 7,799
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H.R.4132 - FAST ActIntroduced Mar 09, 2012 (112th congress) 26 Views
To amend section 506 of the Federal Food, Drug, and Cosmetic Act to expedited approval of drugs for serious or life-threatening diseases or co...
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H.R.4056 - Science and Technology Regulatory Relief Act of 2012Introduced Feb 16, 2012 (112th congress) 5 Views
To amend the Federal Food, Drug, and Cosmetic Act to prevent a State or political subdivision thereof from conducting or requiring duplicative...
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S.2113 - Transforming the Regulatory Environment to Accelerate Access to TreatmentsIntroduced Feb 15, 2012 (112th congress) 4 Views
A bill to empower the Food and Drug Administration to ensure a clear and effective pathway that will encourage innovative products to benefit ...
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H.R.3975Introduced Feb 10, 2012 (112th congress) 10 Views
To amend title V of the Federal Food, Drug, and Cosmetic Act to extend the provisions of the Pediatric Medical Device Safety and Improvement Act.
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H.R.3988 - Generic Drug and Biosimilar User Fee Act of 2012Introduced Feb 10, 2012 (112th congress) 15 Views
To amend the Federal Food, Drug, and Cosmetic Act to establish user-fee programs for generic drugs and biosimilars.
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H.R.3891 - Spending Reductions through Innovations in Therapies Agenda Act of 2012Introduced Feb 02, 2012 (112th congress) 6 Views
To amend the Public Health Service Act to speed American innovation in research and drug development for the leading causes of death that are ...
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S.2069 - Spending Reductions through Innovations in Therapies Agenda Act of 2012Introduced Feb 02, 2012 (112th congress) 11 Views
A bill to amend the Public Health Service Act to speed American innovation in research and drug development for the leading causes of death th...
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H.R.3839 - Drug Shortage Prevention Act of 2012Introduced Feb 16, 2012 (112th congress) 19 Views
To address critical drug shortages.
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H.R.3847 - Safety Of Untested and New Devices Act of 2012Introduced Jan 31, 2012 (112th congress) 19 Views
To amend the Federal Food, Drug, and Cosmetic Act to ensure that a medical device is not marketed based on a determination that the device is ...
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H.R.3737 - ULTRAIntroduced Dec 23, 2011 (112th congress) 14 Views
To amend the Federal Food, Drug, and Cosmetic Act with respect to fast track approval of certain orphan drugs.
