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Food and Drug Administration Amendments Act
Results: 135

#	Item
61	Food and Drug Administration FY 2013 Congressional Budget Request Table of Contents Add to Reading List Source URL: www.fda.gov Language: English Health New Drug Application FluMist Federal Food Drug and Cosmetic Act Influenza vaccine Dietary supplement Pharmaceutical industry Center for Food Safety and Applied Nutrition Food and Drug Administration Amendments Act Food and Drug Administration Medicine Pharmaceutical sciences
62	Appropriations Language Analysis 1 Add to Reading List Source URL: www.fda.gov Language: English Health Pharmacology Pharmaceuticals policy Therapeutics United States Public Health Service Biosimilar Food and Drug Administration Amendments Act Food and Drug Administration Modernization Act Food and Drug Administration Food law Pharmaceutical sciences
63	Current Law User Fees ($5,244,000) in User Fees 1. Why are these amounts necessary? FDA user fee programs help bring safe and effective medical devices, human and animal drugs, biological products, and other FDA-regulate Add to Reading List Source URL: www.fda.gov Language: English Medicine Pharmaceutical sciences Food law Prescription Drug User Fee Act Federal Food Drug and Cosmetic Act Abbreviated New Drug Application Center for Devices and Radiological Health Food and Drug Administration Amendments Act Food and Drug Administration Modernization Act Food and Drug Administration Pharmaceuticals policy Health
64	THE COMMITTEE ON ENERGY AND COMMERCE MEMORANDUM April 5, 2013 To: Health Subcommittee Add to Reading List Source URL: docs.house.gov Language: English - Date: 2013-04-05 14:41:46 Clinical research Pharmaceuticals policy Pharmacology United States Department of Health and Human Services United States Public Health Service Center for Veterinary Medicine Prescription Drug User Fee Act Food and Drug Administration Amendments Act Food and Drug Administration Pharmaceutical sciences Health
65	Cosponsor H.R. 2725, The Lance/Eshoo FDA Safety Over Sequestration (FDA SOS) Act Last year, Congress passed the landmark Food and Drug Administration Safety and Innovation Act of[removed]FDASIA), which included a number of Add to Reading List Source URL: www.ihif.org Language: English - Date: 2013-07-31 12:45:12 Pharmaceuticals policy Food and Drug Administration Pharmaceutical industry Therapeutics Biosimilar Anna Eshoo Generic drug Food and Drug Administration Amendments Act Prescription Drug User Fee Act Pharmaceutical sciences Pharmacology Clinical research
66	Federal Register / Vol. 74, No[removed]Tuesday, April 14, [removed]Notices meetings conducted under the BPCA can be found on the BPCA Web site listed above. The ‘‘New’’ BPCA Title V of Public Law 110–85, the Best Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2014-07-18 11:13:55 Health Government Lake Berryessa National Institute of Child Health and Human Development U.S. Immigration and Customs Enforcement Food and Drug Administration Amendments Act Secure Communities and administrative immigration policies National Institutes of Health Medicine United States Department of Homeland Security
67	2014 FDA Justification of Estimates for Appropriations Committees Add to Reading List Source URL: www.fda.gov Language: English Food and drink Pharmaceuticals policy Medicine Food Safety Modernization Act Center for Food Safety and Applied Nutrition Food safety Federal Food Drug and Cosmetic Act Food Safety and Modernization Act Food and Drug Administration Amendments Act Food and Drug Administration Health Food law
68	Executive Summary Intro FY 2012 Congressional Justification Add to Reading List Source URL: www.fda.gov Language: English Pharmacology Health policy Clinical pharmacology Therapeutics United States Public Health Service United States Department of Health and Human Services Prescription Drug User Fee Act Food and Drug Administration Amendments Act Food and Drug Administration Pharmaceutical sciences Clinical research
69	K to30213 510(K) SUMMARY This 510(k) summary is being submitted in accordance with the Medical Device Amendments of 1976, the requirements of the Safe Medical Devices Act (SMDA) of 1990 and 21 CFR[removed]. Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2011-07-25 00:32:55 Food and Drug Administration Medical technology Pharmaceutical industry Pharmaceuticals policy Food law Medical device Center for Devices and Radiological Health Premarket approval Federal Food Drug and Cosmetic Act Medicine Technology Health
70	Clinical Trials Registration Policy Type: Administrative Responsible Office: Office of Research, Office of Sponsored Programs Initial Policy Approved: [removed]Current Revision Approved: [removed] Add to Reading List Source URL: www.assurance.vcu.edu Language: English - Date: 2014-04-22 08:11:49 Medicine Health Pharmacology Food and Drug Administration Drug safety Clinical trial ClinicalTrials.gov Food and Drug Administration Amendments Act New Drug Application Clinical research Research Pharmaceutical industry

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