Product Description In todays contemporary pharmaceutical industry, the focus has slowly but surely shifted from the elusive research pipeline and latest blockbuster molecules to current processes, efficiencies and manufacturing systems. A path most often taken by manufacturers today in this direction includes improving their overall quality and compliance efforts. This results in a two-pronged approach of minimizing the litigation cost and concurrently improving the overall quality of the products and efficiencies in their processes and procedures. This book provides current thinking and approaches to achieving quality and compliance from top industry experts and is pioneering in bringing this wealth of information together in a single volume which will be of great use to the pharmaceutical industry. Compliance and quality issues have been comprehensively covered, from GMP requirements to deviation management, OOS and CAPA methodologies, QRM and QMS practical implementation, qualification and validation, records and documentation practices, latest GMP training techniques and performance metrics for compliance and detailed analysis of ICH guidelines for practical implementation. This book aligns with the FDA s 21st century initiative and the ICH guidelines focused on quality risk management (ICH Q8, Q9, Q10 and Q11) and underpins the importance of science based decisions and risk evaluation as the centerpiece of compliance policy and execution. It provides a pragmatic framework for establishing a robust quality system. CONTENTS 1 Fundamentals of Global GMP Requirements 2 Effective CAPA Management for Optimal Compliance 3 Laboratory Compliance and Handling Out-of-Specification (OOS) Results in the Laboratory 4 Effectively Incorporating Quality Risk Management into Quality Systems 5 Monitoring and Controlling Process Drift for Enhancing Quality 6 Qualification and Validation 7 Process Validation 8 Documents, Records, and Part 11 Compliance 9 Change Control and Ma