Handbook of Analytical Method Validation for Pharmaceuticals : A Practical Guide to Validating Assay, Impurities, Dissolution, and Residual Solvents Using HPLC and GC

Napte, Bhaskar

ISBN 10: 9373108050 / ISBN 13: 9789373108056

Published by Blue Rose Publishers, 2025

About this Item

Zustand: Sehr gut | Seiten: 266 | Sprache: Englisch | Produktart: Bücher | Handbook of Analytical Method Validation for Pharmaceuticals- A practical guide to validating assay, impurities, dissolution, and residual solvents usingHPLC and GCDesigned for pharmaceutical professionals, this practical handbook serves as a step-by-stepguide to mastering analytical method validation. Covering key parameters such as assay, related substances, dissolution, and residual solvents, the book provides clear insights onusing 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 conceptswith real-world examples, easy-to-follow protocols, and best practices drawn from decades ofindustry experience.What You'll Learn: 1. How to validate analytical methods for various pharmaceutical tests2. Step-by-step guidance on selecting performance characteristics3. Practical tips for setting concentration levels and preparing validation protocols4. How to conduct forced degradation studiesThis book is a must-have resource for professionals working in quality control, analyticalR&D, and regulatory affairs.

Seller Inventory # 43794902/2

Bibliographic Details

• Title: Handbook of Analytical Method Validation for Pharmaceuticals : A Practical Guide to Validating Assay, Impurities, Dissolution, and Residual Solvents Using HPLC and GC
• Publisher: Blue Rose Publishers
• Publication Date: 2025
• Language: English
• ISBN 10: 9373108050
• ISBN 13: 9789373108056
• Binding: Soft cover
• Condition: Sehr gut
• Seller catalogs:
  • Bücher

About this title

Synopsis

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.

About the Author

Bhaskar Napte is an industry expert with 20+ years of experience in analytical sciences, having worked with global pharma giants like Dr. Reddy's, Glenmark, USV, and Apotex. He now leads Pharma Growth Hub, where he trains and mentors professionals throughwebinars, coaching, and now, this practical book-crafted to empower the next generation ofpharma talent..