Handbook of Analytical Method Validation for Pharmaceuticals
A Practical Guide to Validating Assay, Impurities, Dissolution, and Residual Solvents Using HPLC and GC
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Handbook of Analytical Method Validation for Pharmaceuticals - A practical guide to validating assay, impurities, dissolution, and residual solvents using HPLC and GC Designed for pharmaceutical professionals, this practical handbook serves as a step-by-step guide to mastering analytical method validation. Covering key parameters such as assay, related substances, dissolution, and residual solvents, the book provides clear insights on using HPLC and GC techniques in compliance with regulatory expectations. Whether you are validating a method for the first time or looking to deepen your experti...
Handbook of Analytical Method Validation for Pharmaceuticals - A practical guide to validating assay, impurities, dissolution, and residual solvents using HPLC and GC Designed for pharmaceutical professionals, this practical handbook serves as a step-by-step guide to mastering analytical method validation. Covering key parameters such as assay, related substances, dissolution, and residual solvents, the book provides clear insights on using HPLC and GC techniques in compliance with regulatory expectations. Whether you are validating a method for the first time or looking to deepen your expertise, this guide bridges the gap between theory and application. It simplifies complex concepts with real-world examples, easy-to-follow protocols, and best practices drawn from decades of industry experience. What You'll Learn: 1. How to validate analytical methods for various pharmaceutical tests 2. Step-by-step guidance on selecting performance characteristics 3. Practical tips for setting concentration levels and preparing validation protocols 4. How to conduct forced degradation studies This book is a must-have resource for professionals working in quality control, analytical R&D, and regulatory affairs.