Bioequivalence and Statistics in Clinical Pharmacology (Chapman & Hall/CRC Biostatistics Series) by Byron Jones
Bioequivalence and Statistics in Clinical Pharmacology (Chapman & Hall/CRC Biostatistics Series) by Byron Jones
English | Nov 10, 2005 | ISBN: 1584885300 | 384 Pages | PDF | 4 MB
English | Nov 10, 2005 | ISBN: 1584885300 | 384 Pages | PDF | 4 MB
Maintaining a practical perspective, Bioequivalence and Statistics in Clinical Pharmacology explores statistics used in day-to-day clinical pharmacology work. The book 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 proposed 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, they move on to related topics in clinical pharmacology involving the use of cross-over designs.