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Bioequivalence
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#	Item
841	Guidance for Industry Waiver of In Vivo Bioavailability and Bioequivalence Studies for Immediate-Release Solid Oral Dosage Forms Based on a Biopharmaceutics Classification System Add to Reading List Source URL: www.fda.gov Language: English Medicinal chemistry Pharmaceutical industry Clinical research Biopharmaceutics Classification System Bioavailability Dissolution testing Absorption Bioequivalence Drug discovery Pharmaceutical sciences Pharmacology Pharmacokinetics
842	DIVISION OF BIOEQUIVALENCE REVIEW Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical industry Pharmaceutics Axitinib Benzamides Pyridines Thioethers Bioequivalence Clinical trial Dissolution testing Chemistry Organic chemistry Clinical research
843	Guidance for Industry Bioavailability and Bioequivalence Studies for Orally Administered Drug Products — General Considerations U.S. Department of Health and Human Services Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutics Pharmaceutical industry Clinical research Pharmaceuticals policy Bioequivalence Bioavailability Abbreviated New Drug Application Dissolution testing Generic drug Pharmaceutical sciences Pharmacology Pharmacokinetics
844	19851se5-028 BPCA Lotensin Review Add to Reading List Source URL: www.fda.gov Language: English ACE inhibitors Chemistry Lactams Enantiopure drugs Benazepril prodrugs Bioequivalence Bioavailability Pharmacology Pharmacokinetics Pharmaceutical sciences
845	Microsoft Word - 1923dft.doc Add to Reading List Source URL: www.fda.gov Language: English Pharmacokinetics Clinical research Pharmacy Lactams Clinical pharmacology Food and Drug Administration Adverse effect Bioequivalence Bioavailability Pharmaceutical sciences Pharmacology Medicine
846	DIVISION OF BIOEQUIVALENCE REVIEW Add to Reading List Source URL: www.fda.gov Language: English Clobazam Bioequivalence Dissolution testing Chemistry Organochlorides Benzodiazepines Lactams
847	Guidance for Industry Dissolution Testing of Immediate Release Solid Oral Dosage Forms U.S. Department of Health and Human Services Food and Drug Administration Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutics Pharmacokinetics Clinical research Food and Drug Administration Biopharmaceutics Classification System Dissolution testing IVIVC Bioequivalence Abbreviated New Drug Application Pharmaceutical sciences Pharmacology Pharmaceutical industry
848	Guidance for Industry #35 - Bioequivalence Guidance, revised November, 8, 2006 Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutics Bioequivalence Abbreviated New Drug Application Food and Drug Administration Cmax Dissolution testing Bioavailability Methadone Pharmaceutical sciences Pharmacology Pharmacokinetics
849	Guidance for Industry Bioavailability and Bioequivalence Studies for Orally Administered Drug Products — General Considerations DRAFT GUIDANCE Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutics Pharmaceutical industry Pharmaceuticals policy Clinical research Bioequivalence Bioavailability Generic drug Abbreviated New Drug Application Dissolution testing Pharmaceutical sciences Pharmacology Pharmacokinetics
850	Microsoft Word[removed]5rev.DOC Add to Reading List Source URL: www.fda.gov Language: English Medicine Clinical research Pharmaceutical industry Drug safety Pharmacokinetics Generic drug Investigational New Drug Abbreviated New Drug Application Bioequivalence Pharmaceutical sciences Pharmacology Food and Drug Administration

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