ABSTRACT

Describes analytical methods development, optimization and validation, and provides examples of successful methods development and validation in high-performance liquid chromatography (HPLC) areas. The text presents an overview of Food and Drug Administration (FDA)/International Conference on Harmonization (ICH) regulatory guidelines, compliance with validation requirements for regulatory agencies, and methods validation criteria stipulated by the US Pharmacopia, FDA and ICH.

chapter |4 pages

Preface

chapter |4 pages

Contents

part |2 pages

Tables and Figures

chapter |4 pages

Abbreviations

chapter 1|36 pages

Introduction

chapter 3|20 pages

Method Validation (USP/ICH)

part 4|2 pages

System Suitability

chapter 5|6 pages

Method Validation Protocol

part 6|2 pages

Method Transfer and Revalidation

chapter 7|2 pages

Summary and Conclusions