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Drug user
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541	OMB INFORMATION COLLECTION SUPPORTING STATEMENT New Drug and Biological Drug Products; Evidence Needed to Demonstrate Efficacy of New Drugs for Use Against Lethal or Permanently Disabling Toxic Substances When Efficacy S Add to Reading List Source URL: www.fda.gov Language: English - Date: 2000-01-07 07:23:47 Pharmaceutical sciences Center for Biologics Evaluation and Research New Drug Application Regulatory requirement Biologic License Application Center for Drug Evaluation and Research Title 21 of the Code of Federal Regulations Biologic Prescription Drug User Fee Act Food and Drug Administration Medicine Health
542	1701 K Street, PnoNE[removed]NW, Suite[removed] Add to Reading List Source URL: www.fda.gov Language: English - Date: 2006-01-03 18:15:55 Pharmaceutical sciences Medicine Prescription Drug User Fee Act Direct-to-consumer advertising Food and Drug Administration Amendments Act Food and Drug Administration Modernization Act Food and Drug Administration Pharmaceuticals policy Health
543	0 October 18, 2004 Division of Dockets Management (HFA-305) Food and Drug Administration 5630 Fishers Lane, Room 1061 Rockville, MD 20852 Add to Reading List Source URL: www.fda.gov Language: English - Date: 2004-11-05 15:37:47 Research Pharmacology Clinical research Pharmaceutical industry Medical statistics New Drug Application Clinical trial Investigational New Drug Prescription Drug User Fee Act Food and Drug Administration Health Pharmaceutical sciences
544	DOC Document Add to Reading List Source URL: www.maine.gov Language: English - Date: 2013-11-19 13:50:49 Drug rehabilitation Substance abuse Form Buprenorphine Organic chemistry Chemistry User interface techniques Drug addiction
545	Statementof the National Center for Policy Research(CPR) for Women & Families At the FDA Meeting on Risk Management for Prescription Drugs & FAMILIES Add to Reading List Source URL: www.fda.gov Language: English - Date: 2002-11-06 16:09:34 Pharmaceuticals policy Health Prescription Drug User Fee Act Direct-to-consumer advertising Pharmaceutical industry Adverse Event Reporting System Norfloxacin Prescription medication Criticism of the Food and Drug Administration Pharmaceutical sciences Food and Drug Administration Pharmacology
546	EXECUTIVE SUMMARY The Medical Device User Fee Amendments (MDUFA, formally referred to as MDUFMA), as amended, requires the Food and Drug Administration (FDA) to report annually on the financial aspects of its implementa Add to Reading List Source URL: www.fda.gov Language: English Food and Drug Administration Pharmacology Therapeutics United States Public Health Service Pharmaceutical sciences Clinical research Clinical pharmacology
547	mc MILLER REPORTING COMPANY, INC. 735 8th Street, S.E. Washington, D.C[removed]-6666 TCBDEPARTMENT OF HEALTH AND HUMAN SERVICES Add to Reading List Source URL: www.fda.gov Language: English - Date: 2000-10-04 08:23:36 Health Medicine Pharmacology Prescription Drug User Fee Act Food law Pharmaceutical industry Food and Drug Administration Modernization Act New Drug Application Center for Drug Evaluation and Research Food and Drug Administration Pharmaceuticals policy Pharmaceutical sciences
548	PDF Document Add to Reading List Source URL: www.fda.gov Language: English - Date: 2006-01-03 18:15:54 Pharmaceuticals policy Medicine Food and Drug Administration Clinical pharmacology United States Public Health Service Prescription Drug User Fee Act Direct-to-consumer advertising Pharmaceutical industry Prescription medication Pharmacology Pharmaceutical sciences Health
549	, Merck & Co.,Inc. PO.Box4, BLA-20 West PointPA19486 Tel[removed][removed] Add to Reading List Source URL: www.fda.gov Language: English - Date: 1999-09-20 08:30:57 Pharmaceutical industry Pharmaceuticals policy Food and Drug Administration Validity Validation Prescription Drug User Fee Act Merck & Co. Pharmaceutical sciences Pharmacology Clinical research
550	SMG[removed]FDA STAFF MANUAL GUIDES, VOLUME II - DELEGATIONS OF AUTHORITY REGULATORY - GENERAL REDELEGATIONS OF AUTHORITY EMERGENCY FUNCTIONS Effective Date: [removed] Add to Reading List Source URL: www.fda.gov Language: English Pharmacology Office of Regulatory Affairs FDA Criticism of the Food and Drug Administration Prescription Drug User Fee Act Food and Drug Administration Pharmaceutical sciences Clinical research

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