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Dissolution testing
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121	PDF Document Add to Reading List Source URL: www.fda.gov Language: English Dosage forms Medicine Quality control Dissolution testing Food and Drug Administration Prednisone Tablet Center for Drug Evaluation and Research Technical standard Pharmaceutical industry Pharmacology Pharmaceutical sciences
122	PDF Document Add to Reading List Source URL: www.anbex.com Language: English - Date: 2006-07-07 11:23:55 Pharmaceutical industry Pharmacology Dosage forms Potassium compounds Disaster preparedness Potassium iodide Shelf life Food and Drug Administration Dissolution testing Medicine Health Chemistry
123	Example QbD MR Tablet Module 3 Quality 3.2.P.2 Pharmaceutical Development Quality by Design for ANDAs: An Example for Modified Release Dosage Forms Introduction to the Example Add to Reading List Source URL: www.fda.gov Language: English Dosage forms Chemistry Tablet Excipient Time release technology Quality by Design Formulation Dissolution testing Capsule Pharmacology Pharmaceutical sciences Pharmaceutical industry
124	Microsoft Word - 10472dft.doc Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical industry Pharmacokinetics Clinical research Drug safety Bioequivalence Abbreviated New Drug Application Food and Drug Administration Dissolution testing New Drug Application Pharmaceutical sciences Pharmacology Pharmaceutics
125	DIVISION OF BIOEQUIVALENCE REVIEW Add to Reading List Source URL: www.fda.gov Language: English Phenols Organofluorides Chemistry Ezetimibe Pharmacology Pharmaceutics Statin Bioequivalence Dissolution testing Merck Pharmaceutical industry Schering-Plough
126	Guidance for Industry Extended Release Oral Dosage Forms: Development, Evaluation, and Application of In Vitro/In Vivo Correlations Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical industry Dissolution testing Quality control Pharmacokinetics IVIVC Bioequivalence In vitro Abbreviated New Drug Application Food and Drug Administration Pharmaceutical sciences Pharmacology Pharmaceutics
127	Guidance for Industry Immediate Release Solid Oral Dosage Forms Scale-Up and Postapproval Changes: Chemistry, Manufacturing, and Controls, In Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutics Clinical research Dosage forms Pharmacokinetics Dissolution testing Bioequivalence Food and Drug Administration Excipient Generic drug Pharmaceutical sciences Pharmaceutical industry Pharmacology
128	Microsoft Word - 071368C1007 Add to Reading List Source URL: www.fda.gov Language: English Membrane biology Pharmaceutical industry Antifungals Amphotericin B Bioequivalence Liposome Dissolution testing Abbreviated New Drug Application Generic drug Pharmacology Pharmaceutical sciences Pharmacokinetics
129	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
130	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

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