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OverviewFull Product DetailsAuthor: Kate McCormick , D. Wylie McVay JrPublisher: Taylor & Francis Ltd Imprint: Routledge Edition: New edition Weight: 0.757kg ISBN: 9781409427117ISBN 10: 1409427110 Pages: 288 Publication Date: 28 July 2012 Audience: Professional and scholarly , College/higher education , Professional & Vocational , Postgraduate, Research & Scholarly Format: Hardback Publisher's Status: Active Availability: In Print  This item will be ordered in for you from one of our suppliers. Upon receipt, we will promptly dispatch it out to you. For in store availability, please contact us. Table of ContentsReviews'...a valuable resource for those seeking information on the modern approach to pharmaceutical production. If your aim is to employ a scientific and risk-based approach to the manufacturing process while maximising profit and ensuring customer satisfaction, then Pharmaceutical Process Design and Management should form part of your reference material.' Quality World Author InformationKate McCormick has extensive experience in pharmaceutical manufacturing, having worked with companies and regulators worldwide. She has published several textbooks and articles, edited GMP Review from 2004 to 2011 and is a former education advisor for ISPE. McCormick has qualifications in biochemistry, microbiology and business studies. Wylie McVay has extensive operations support experience in pharmaceutical quality control, quality assurance and post-approval regulatory affairs. McVay is a review board member of the Journal of Validation Technology and GxP Compliance magazines. He is certified in Quality and Regulatory and holds a Master of Science in Quality Assurance and Regulatory Affairs. Tab Content 6Author Website:Countries AvailableAll regions |
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