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Verlag: Chapman and Hall/CRC, 2016
ISBN 10: 146658520XISBN 13: 9781466585201
Anbieter: GreatBookPrices, Columbia, MD, USA
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Zustand: New.
Verlag: Taylor and Francis Inc, 2016
ISBN 10: 146658520XISBN 13: 9781466585201
Anbieter: PBShop.store US, Wood Dale, IL, USA
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HRD. Zustand: New. New Book. Shipped from UK. Established seller since 2000.
Verlag: CRC Press 2017-01-12, Boca Raton, 2017
ISBN 10: 146658520XISBN 13: 9781466585201
Anbieter: Blackwell's, London, Vereinigtes Königreich
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hardback. Zustand: New. Language: ENG.
Verlag: Chapman and Hall/CRC, 2016
ISBN 10: 146658520XISBN 13: 9781466585201
Anbieter: GreatBookPrices, Columbia, MD, USA
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Zustand: As New. Unread book in perfect condition.
Verlag: Chapman and Hall/CRC, 2016
ISBN 10: 146658520XISBN 13: 9781466585201
Anbieter: Brook Bookstore, Milano, MI, Italien
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Zustand: new.
Verlag: Chapman and Hall/CRC, 2016
ISBN 10: 146658520XISBN 13: 9781466585201
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Zustand: New.
Verlag: Chapman and Hall/CRC 2017-01-12, 2017
ISBN 10: 146658520XISBN 13: 9781466585201
Anbieter: Chiron Media, Wallingford, Vereinigtes Königreich
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Hardcover. Zustand: New.
Verlag: CRC Press, 2016
ISBN 10: 146658520XISBN 13: 9781466585201
Anbieter: PBShop.store UK, Fairford, GLOS, Vereinigtes Königreich
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HRD. Zustand: New. New Book. Shipped from UK. Established seller since 2000.
Verlag: Chapman and Hall/CRC, 2016
ISBN 10: 146658520XISBN 13: 9781466585201
Anbieter: GreatBookPricesUK, Castle Donington, DERBY, Vereinigtes Königreich
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Zustand: As New. Unread book in perfect condition.
Verlag: Taylor & Francis Inc, Bosa Roca, 2016
ISBN 10: 146658520XISBN 13: 9781466585201
Anbieter: CitiRetail, Stevenage, Vereinigtes Königreich
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Hardcover. Zustand: new. Hardcover. Maintaining a practical perspective, Bioequivalence and Statistics in Clinical Pharmacology, Second Edition explores statistics used in day-to-day clinical pharmacology work. The book is a starting point for those involved in such research and covers the methods needed to design, analyze, and interpret bioequivalence trials; explores when, how, and why these studies are performed as part of drug development; and demonstrates the methods using real world examples. Drawing on knowledge gained directly from working in the pharmaceutical industry, the authors set the stage by describing the general role of statistics. Once the foundation of clinical pharmacology drug development, regulatory applications, and the design and analysis of bioequivalence trials are established, including recent regulatory changes in design and analysis and in particular sample-size adaptation, they move on to related topics in clinical pharmacology involving the use of cross-over designs. These include, but are not limited to, safety studies in Phase I, dose-response trials, drug interaction trials, food-effect and combination trials, QTc and other pharmacodynamic equivalence trials, proof-of-concept trials, dose-proportionality trials, and vaccines trials. This second edition addresses several recent developments in the field, including new chapters on adaptive bioequivalence studies, scaled average bioequivalence testing, and vaccine trials.Purposefully designed to be instantly applicable, Bioequivalence and Statistics in Clinical Pharmacology, Second Edition provides examples of SAS and R code so that the analyses described can be immediately implemented. The authors have made extensive use of the proc mixed procedures available in SAS. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability.
Verlag: Chapman & Hall, 2016
ISBN 10: 146658520XISBN 13: 9781466585201
Anbieter: Revaluation Books, Exeter, Vereinigtes Königreich
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Hardcover. Zustand: Brand New. 2nd edition. 434 pages. 10.50x7.00x1.00 inches. In Stock.
Verlag: Chapman and Hall/CRC, 2016
ISBN 10: 146658520XISBN 13: 9781466585201
Anbieter: Palexbooks, Miami, FL, USA
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Zustand: New. Brand new! Please provide a physical shipping address.