Catatan

This book is About Historical Development of Dissolution Testing, Compendial Testing Equipment: Calibration, Qualification, and Sources of Error, Compendial Requirements of Dissolution Testing—European Pharmacopoeia, Japanese Pharmacopoeia, United States Pharmacopeia, The Role of Dissolution Testing in the Regulation of Pharmaceuticals: The FDA Perspective, Gastrointestinal Transit and Drug Absorption, Physiological Parameters Relevant to Dissolution Testing: Hydrodynamic Considerations, Development of Dissolution Tests on the Basis of Gastrointestinal Physiology, Orally Administered Drug Products: Dissolution Data Analysis with a View to In Vitro–In Vivo Correlation, Interpretation of In Vitro–In Vivo Time Profiles in Terms of Extent, Rate, and Shape, Study Design Considerations for IVIVC Studies, Dissolution Method Development with a View to Quality Control, Dissolution Method Development: An Industry Perspective, Design and Qualification of Automated Dissolution Systems, Bioavailability of Ingredients in Dietary Supplements: A Practical Approach to the In Vitro Demonstration of the Availability of Ingredients in Dietary Supplements.