The Series is a comprehensive reference for the pharmaceutical professional covering all aspects from , documentation and validation through manufacturing processes to facility design and management. In ‘’, Dr Kate McCormick provides the reader with comprehensive coverage of this vital subject, including the life cycle, management and cost of , GMP, auditing and inspections. This book with the others in the series will become a unique source of reference and educational material for the readership.

Case studies and examples make the book of direct practical relevance to the professional in the pharmaceutical industry Find the answers you are looking for quickly and easily with clear indexing and referencing Reference to international standards and practice mean this book will be useful wherever you are working.