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OverviewThe Pharmaceutical Engineering Series is a comprehensive reference for the pharmaceutical professional covering all aspects from quality, documentation and validation through manufacturing processes to facility design and management. In 'Quality', Dr Kate McCormick provides the reader with comprehensive coverage of this vital subject, including the quality life cycle, management and cost of quality, 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. Full Product DetailsAuthor: Kathleen E. McCormick (Pharmaceutical Consultant, Devon, UK)Publisher: Elsevier Science & Technology Imprint: Butterworth-Heinemann Ltd Volume: v. 2 Dimensions: Width: 17.10cm , Height: 1.50cm , Length: 24.40cm Weight: 0.810kg ISBN: 9780750651134ISBN 10: 075065113 Pages: 275 Publication Date: 23 July 2002 Audience: Professional and scholarly , Professional & Vocational Format: Hardback Publisher's Status: Out of Print Availability: In Print ![]() Limited stock is available. It will be ordered for you and shipped pending supplier's limited stock. Table of ContentsQuality Life Cycle Quality Assurance and Quality Control Quality Systems Good Manufacturing Practice Management of Quality Cost of Quality Qualified Person Technology Transfer Calibration Auditing/Inspections Pharmaceutical Microbiology Quality Improvement Programmes Quality Tools and TechniquesReviewsKate McCormick has here provided a valuable and very readable overview of quality management in the pharmaceutical industry... This volume provides much useful information in a very concise format. It therefore goes straight onto my shortlist of recommended reading for chemists interested in GMP. Organic Process Research and Development Journal Part of the pharmaceutical engineering series, Kate McCormick's book delivers comprehensive coverage of the quality side of the subject area... This is an easy to read reference to what is a complex subject and billed as an essential addition to the pharmaceutical professional's bookshelf. Quality World, Dec 2002 Author InformationDr. Kate McCormick is a pharmaceutical manufacturing consultant and trainer who has worked extensively with both regulators and companies in more than 50 countries. She is the author of a number of textbooks, and she was an editor of GMP Review and International Education Advisor for ISPE. Dr. McCormick has a degree in biochemistry, a doctorate in microbiology, and is also a Master of Business Administration. Tab Content 6Author Website:Countries AvailableAll regions |