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Pharmaceutical dissolution testing / edited by Jennifer Dressman, Johannes Krämer.

Contributor(s): Dressman, J. B | Krämer, Johannes.
Material type: TextTextPublisher: Boca Raton : Taylor & Francis, c2005Description: xv, 429 p. : ill. ; 24 cm.ISBN: 9780824754679 (alk. paper); 0824754670 (alk. paper).Subject(s): Drugs -- Solubility -- Testing | Dosage Forms -- standards | Drug CompoundingDDC classification: 615.19 Online resources: WorldCat details | Ebook Fulltext
Contents:
Table of contents 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
Summary: Pharmaceutical Dissolution Testing
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Item type Current location Collection Call number Copy number Status Date due Barcode Item holds
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Non-fiction 615.19 PHA 2005 (Browse shelf) Not for loan
Text Text EWU Library
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Non-fiction 615.19 PHA 2005 (Browse shelf) C-1 Not For Loan 18426
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Includes bibliographical references and index.

Table of contents 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

Pharmacy

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