Pharmaceutical dissolution testing / edited by Jennifer Dressman, Johannes Krämer.Material type: TextLanguage: English Publication details: Boca Raton : Taylor & Francis, c2005. Description: xv, 429 p. : ill. ; 24 cmISBN: 9780824754679 (alk. paper); 0824754670 (alk. paper)Subject(s): Drugs -- Solubility -- Testing | Dosage Forms -- standards | Drug CompoundingDDC classification: 615.19 LOC classification: RS189 | .P446 2005NLM classification: QV 778Online resources: WorldCat details | Ebook Fulltext
|Item type||Current library||Collection||Call number||Copy number||Status||Date due||Barcode||Item holds|
|E-Book||EWU Library E-book||Non-fiction||615.19 PHA 2005 (Browse shelf(Opens below))||Not for loan|
|Text||EWU Library Reserve Section||Non-fiction||615.19 PHA 2005 (Browse shelf(Opens below))||C-1||Not For Loan||18426|
Includes bibliographical references and index.
TOC Historical Development of Dissolution Testing. Compendial Testing Equipment: Calibration, Qualification, and Sources of Error. Compendial Requirements of Dissolution Testing. The Role of Dissolution Testing in the Regulation of Pharmaceuticals: The FDA Perspective. Physiological Parameters Relevant to Dissolution Testing: Composition of Fluids in the GI Tract. Physiological Parameters Relevant to Dissolution Testing: Hydrodynamic Considerations. Physiological Parameters Relevant to Dissolution Testing: Behavior of Solid Pharmaceuticals in the GI Tract. Dissolution Data Analysis with a View to IVIVC. Analysis and Interpretation of Time Profiles In Vitro and In Vivo. Pharmacokinetic Study Design with a View to Quality Control. Dissolution Method Development: An Industrial Perspective. Design and Qualification of Automated Dissolution Systems
Pharmaceutical Dissolution Testing
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