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Bioequivalence
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351	Clinical Approach to Safety and Surveillance of Generic Drugs Add to Reading List Source URL: www.fda.gov Language: English Clinical research Pharmaceutical industry Drug safety Pharmaceuticals policy Food and Drug Administration Generic drug Bioequivalence Abbreviated New Drug Application Pharmacovigilance Pharmaceutical sciences Pharmacology Research
352	Guidance on Bioequivalence Studies for Reproductive Health Medicines WHO Prequalification of Medicines Programme Add to Reading List Source URL: apps.who.int Language: English - Date: 2014-11-27 08:53:52 Research Pharmaceutical industry Pharmacokinetics Pharmaceuticals policy Bioequivalence Generic drug Clinical trial Abbreviated New Drug Application International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Pharmaceutical sciences Pharmacology Clinical research
353	WHO Prequalification of Medicines Programme Guidance Document 14 August 2014 Add to Reading List Source URL: apps.who.int Language: English - Date: 2014-08-14 05:16:26 Pharmacy Electronic circuits Clinical research Pharmaceutical industry Comparator Bioequivalence Tablet Pharmacology Pharmaceutical sciences Dosage forms
354	Microsoft Word - E.01 CMDv report for release November 2008 Final Add to Reading List Source URL: www.hma.eu Language: English - Date: 2008-12-10 12:07:45 Pharmaceutics Pharmacology European Medicines Agency Westferry DLR station Validation Bioequivalence Clinical research Pharmaceutical industry Research
355	CENTRAL REGION Bioequivalence Laboratory Bioequivalence & Testing Centre Universiti Malaya (UM) Conducts analysis of drug levels in plasma for bioequivalence Add to Reading List Source URL: www.biotechcorp.com.my Language: English - Date: 2013-12-02 11:47:08 Bioavailability Clinical pharmacology Pharmacology ADME Pharmacokinetics Pharmaceutical sciences Bioequivalence
356	DIVISION OF BIOEQUIVALENCE REVIEW Add to Reading List Source URL: www.fda.gov Language: English Anatomy Biology Digestive system Bile acids Bile acid Colestipol Cholestyramine Bile Lysergic acid diethylamide Hepatology Medicine Bile acid sequestrants
357	Generic Drug User Fee Amendments of 2012 Regulatory Science Initiatives: Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical industry Food and Drug Administration Center for Drug Evaluation and Research United States Department of Health and Human Services Bioequivalence Drug development Generic drug Pharmaceutical sciences Pharmacology Clinical research
358	asabaliauskas on DSK5VPTVN1PROD with NOTICES Federal Register / Vol. 79, No[removed]Wednesday, September 24, [removed]Notices with premarket review regulations and performance standards under sections 514 and 515 of the FD Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2014-10-07 13:23:43 Pharmacology Pharmaceuticals policy Food and Drug Administration Food law Pharmaceutical industry Bioequivalence Abbreviated New Drug Application International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Federal Food Drug and Cosmetic Act Medicine Clinical research Pharmaceutical sciences
359	Microsoft Word - 2003guidance_redo_10[removed]doc Add to Reading List Source URL: www.fda.gov Language: English Dosage forms Clinical research Pharmacokinetics Medicinal chemistry Bioequivalence Abbreviated New Drug Application Nasal administration Bioavailability Drug delivery Pharmaceutical sciences Pharmacology Medicine
360	#224 GUIDANCE FOR INDUSTRY B IOEQUIVALENCE : B LOOD L EVEL B IOEQUIVALENCE S TUDY VICH GL52 Draft Guidance Add to Reading List Source URL: www.fda.gov Language: English Science Bioequivalence Methadone Clinical trial Dose Specification Phases of clinical research TGN1412 Clinical research Research Chemistry

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