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OverviewFull Product DetailsAuthor: Harry Yang , Steven NovickPublisher: Taylor & Francis Ltd Imprint: CRC Press Weight: 0.825kg ISBN: 9781138295872ISBN 10: 1138295876 Pages: 310 Publication Date: 11 July 2019 Audience: College/higher education , General/trade , Tertiary & Higher Education , General 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 ContentsBackground. Drug Research and Development. Basics of Bayesian analysis. Bayesian Estimation of Sample Size and Power. Pre-Clinical and Clinical Research. Pre-clinical efficacy study. Futility analysis. Phase 3 Clinical Trial. Chemistry, Manufacturing, and Control. Analytical method. Process Development. Bayesian Approach to Statistical Process Control.ReviewsAuthor InformationHarry Yang is Senior Director and Head of Statistical Sciences at MedImmune. He has 24 years of experience across all aspects of drug research and development and extensive global regulatory experiences. He has published six statistical books, 15 book chapters, and over 90 peer-reviewed papers on diverse scientific and statistical subjects, including 15 joint statistical works with Dr. Novick. Dr. Yang is a frequent invited speaker at national and international conferences. He also developed statistical courses and conducted training at the FDA and USP as well as Peking University. Steven Novick is Director of Statistical Sciences at MedImmune. He has extensively contributed statistical methods to the biopharmaceutical literature. Dr. Novick is a skilled Bayesian computer programmer and is frequently invited to speak at conferences, having developed and taught courses in several areas, including drug-combination analysis and Bayesian methods in clinical areas. He served on IPAC-RS and has chaired several national statistical conferences. Tab Content 6Author Website:Countries AvailableAll regions |
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