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Drug user
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271	History of the U.S. Food and Drug Administration Interviewee: Add to Reading List Source URL: www.fda.gov Language: English Health Clinical pharmacology Pharmacology Therapeutics United States Public Health Service Prescription Drug User Fee Act Food and Drug Administration Pharmaceutical sciences Clinical research
272	FY2013 ADUFA Financial Report - Background Add to Reading List Source URL: www.fda.gov Language: English Food and Drug Administration Clinical pharmacology Therapeutics United States Public Health Service Pharmaceutical industry Prescription Drug User Fee Act Pharmaceutical sciences Pharmacology Clinical research
273	FY 2013 BsUFA Financial Report Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences Health Pharmacology Food law Prescription Drug User Fee Act Biosimilar Biologic Federal Food Drug and Cosmetic Act Food and Drug Administration Medicine Pharmaceuticals policy
274	FY 2013 BsUFA Financial Report Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences Health Pharmacology Food law Prescription Drug User Fee Act Biosimilar Biologic Fee Federal Food Drug and Cosmetic Act Food and Drug Administration Pharmaceuticals policy Medicine
275	Update-Summer 2011:Layout[removed]:01 AM Page 1 Look inside for details! by Stephen E. Trimboli, Esq. When Does "Current" Drug Use Add to Reading List Source URL: drugfreenj.org Language: English - Date: 2013-02-26 18:43:25 Drug user Substance abuse Drug test Illegal drug trade Medicine Health Drug control law Law Substance dependence
276	FY 2013 BsUFA Financial Report Add to Reading List Source URL: www.fda.gov Language: English Pharmacology Clinical research Prescription Drug User Fee Act Fee Biosimilar Origination fee Food and Drug Administration Pharmaceuticals policy Pharmaceutical sciences
277	SOPP 8412: Review of Product Labeling Version # 4 Effective Date: April 2, 2012 I. Purpose This SOPP outlines the general operating procedures for Center for Biologics Evaluation and Research (CBER) staff to process draf Add to Reading List Source URL: www.fda.gov Language: English Health Pharmaceuticals policy Pharmacology Food law Structured Product Labeling New Drug Application Prescription Drug User Fee Act Title 21 of the Code of Federal Regulations Pharmaceutical industry Medicine Food and Drug Administration Pharmaceutical sciences
278	MDUFMA FY 2011 Financial Report Add to Reading List Source URL: www.fda.gov Language: English Clinical pharmacology Food and Drug Administration Pharmacology Therapeutics United States Public Health Service Medical device Fee Prescription Drug User Fee Act Medicine Health Pharmaceutical sciences
279	CLINICAL REVIEW Division of Clinical Evaluation, Office of Cellular Tissue and Gene Therapy, Center for Biologics Evaluation and Research; with consultation from the Office of Device Evaluation, Division of Anesthesiolog Add to Reading List Source URL: www.fda.gov Language: English Biology Clinical research Pharmacology Pharmaceutical industry Design of experiments Center for Biologics Evaluation and Research Mucogingival junction Clinical trial Prescription Drug User Fee Act Food and Drug Administration Health Medicine
280	4. USER FEES AND OTHER COLLECTIONS In addition to collecting taxes and other governmental receipts by the exercise of its sovereign powers, the Federal Government earns income from its various business-type activities. E Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2010-09-30 13:19:50 United States federal budget United States budget process Fee Prescription Drug User Fee Act Medicare Government PAYGO United States federal legislation

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