
- 566 pages
- English
- ePUB (mobile friendly)
- Available on iOS & Android
Handbook of Modern Pharmaceutical Analysis
About this book
This book describes the role modern pharmaceutical analysis plays in the development of new drugs. Detailed information is provided as to how the quality of drug products is assured from the point of discovery until the patient uses the drug. Coverage includes state-of-the-art topics such as analytics for combinatorial chemistry and high-throughput screening, formulation development, stability studies, international regulatory aspects and documentation, and future technologies that are likely to impact the field. Emphasis is placed on current, easy-to-follow methods that readers can apply in their laboratories.No book has effectively replaced the very popular text, Pharmaceutical Analysis, that was edited in the 1960s by Tak Higuchi. This book will fill that gap with an up-to-date treatment that is both handy and authoritative.
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Information
Table of contents
- Cover image
- Title page
- Table of Contents
- Front Matter
- Copyright page
- Contributors
- Preface
- Chapter 1: Modern Pharmaceutical Analysis: An Overview
- Chapter 2: Combinatorial Chemistry and High-Throughput Screening in Drug Discovery and Development
- Chapter 3: Solid-State Analysis
- Chapter 4: Degradation and Impurity Analysis for Pharmaceutical Drug Candidates
- Chapter 5: Preformulation Studies
- Chapter 6: Solid Dosage-Form Analysis
- Chapter 7: Parenteral Dosage Forms
- Chapter 8: New Drug Delivery Systems
- Chapter 9: Compendial Testing
- Chapter 10: Method Development
- Chapter 11: Setting Up Specifications
- Chapter 12: Validation of Pharmaceutical Test Methods
- Chapter 13: Stability Studies
- Chapter 14: Analytical Methodology Transfer
- Chapter 15: Pharmaceutical Analysis Documentation
- Chapter 16: An Innovative Separation Platform: Electrophoretic Microchip Technology
- Index