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Dissolution testing
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71	Biorelevant In-Vitro Release Testing of NonOral Dosage Forms – FDA Perspectives Tapash Ghosh, Ph.D Team Leader, Biopharmaceutics, ONDQA, FDA Annual AAPS, San Antonio, Texas November 11, 2013 Disclaimer: The contents of Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical industry Clinical research Pharmacology Food and Drug Administration Dissolution testing IVIVC Pharmaceutical sciences In vivo In vitro
72	Bundesinstitut für Arzneimittel und Medizinprodukte Dissolution testing of herbal medicinal products – Viewpoint of the regulatory authority Add to Reading List Source URL: www.ga-online.org Language: English - Date: 2009-09-27 10:11:55 Pharmacopoeia Medicine Health Federal Institute for Drugs and Medical Devices Council of Europe Dissolution testing
73	DIVISION OF BIOEQUIVALENCE REVIEW Add to Reading List Source URL: www.fda.gov Language: English Medicine Health Hypoglycemia Bioequivalence Dissolution testing
74	„The Practice of Dissolution Testing in Herbal Medicinal Products“ The impact of dosage forms Add to Reading List Source URL: www.ga-online.org Language: English - Date: 2009-09-27 10:12:23 Dissolution Biology Science Dietary supplements Herbalism Herbal
75	Microsoft Word - Discovery BCS Dissolution data sheet.docx Add to Reading List Source URL: tsrlinc.com Language: English - Date: 2011-05-02 15:17:58 Quality control Solutions Gastric acid USP Enzyme Dissolution Assay Solubility Biopharmaceutics Classification System Chemistry Dissolution testing Pharmaceutical industry
76	Regulatory Considerations for Post-Approval Manufacturing Changes and the Utility of Change Protocols – FDA Perspective AAPS Annual Meeting San Antonio, Texas November 12, 2013 Add to Reading List Source URL: www.fda.gov Language: English Medicine Clinical research Clinical pharmacology Food and Drug Administration United States Public Health Service Abbreviated New Drug Application Dissolution testing Bioequivalence Validation Pharmaceutical sciences Pharmaceutical industry Pharmacology
77	CMC Workshop From Drug Development to Global Supply to Patients April 15-17, 2013, Washington, DC Post-Approval Change Management: Challenges and Opportunities – Add to Reading List Source URL: www.fda.gov Language: English Clinical research Clinical pharmacology Food and Drug Administration United States Public Health Service Dissolution testing Abbreviated New Drug Application Bioequivalence New Drug Application Regulatory requirement Pharmaceutical sciences Pharmacology Pharmaceutical industry
78	What are clinically relevant dissolution specifications? Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences In vivo Bioavailability Pharmaceutical industry Dissolution testing Food and Drug Administration IVIVC Pharmacokinetics
79	Microsoft Word - GLP BCS Drug Product Dissolution data sheet.docx Add to Reading List Source URL: tsrlinc.com Language: English - Date: 2011-05-02 16:04:10 Quality control Pharmacology USP Gastric acid Abbreviated New Drug Application Enzyme Aspirin Biopharmaceutics Classification System Chemistry Pharmaceutical industry Dissolution testing
80	What are clinically relevant dissolution specifications? Add to Reading List Source URL: www.fda.gov Language: English Clinical research Bioequivalence Pharmacokinetics In vivo Food and Drug Administration Dissolution testing IVIVC Pharmaceutical sciences Pharmacology Research

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