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Bioequivalence and Statistics in Clinical Pharmacology, Second Edition by Jones, Byron; Patterson, Scott D is a nonfiction available to read on EtoBox.
What is Bioequivalence and Statistics in Clinical Pharmacology, Second Edition about?
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-concep
Who reads Bioequivalence and Statistics in Clinical Pharmacology, Second Edition?
It is typically read by self-directed learners exploring a subject in depth.
Common subject areas: history, science, philosophy, social sciences.
- Author
- Jones, Byron; Patterson, Scott D
- Publisher
- Chapman and Hall/CRC, CRC Press
- Published
- 2017
- Language
- EN
- ISBN
- 9780367782443
- Category
- nonfiction
- Subjects
- Mathematics, Medical, Medicine
Other editions & translations
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