Clinical trials are arguably the most important steps in proving drug effectiveness and safety for public use. They require intensive planning and organization and involve a wide range of disciplines: data management, biostatistics, pharmacology, toxicology, modeling and simulation, regulatory monitoring, ethics, and particular issues for given disease areas. "Clinical Trials Handbook" provides a comprehensive and thorough reference on the basics and practices of clinical trials.
With contributions from a range of international authors, the book takes the reader through each trial phase, technique, and issue. Chapters cover every key aspect of preparing and conducting clinical trials, including:
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Clinical trials are arguably the most important steps in proving drug effectiveness and safety for public use. They require intensive planning and organization and involve a wide range of disciplines: data management, biostatistics, pharmacology, toxicology, modeling and simulation, regulatory monitoring, ethics, and particular issues for given disease areas. "Clinical Trials Handbook" provides a comprehensive and thorough reference on the basics and practices of clinical trials.
With contributions from a range of international authors, the book takes the reader through each trial phase, technique, and issue. Chapters cover every key aspect of preparing and conducting clinical trials, including:
Imprint | John Wiley & Sons |
Country of origin | United States |
Release date | July 2009 |
Availability | Expected to ship within 12 - 17 working days |
First published | July 2009 |
Authors | S.C. Gad |
Dimensions | 257 x 178 x 50mm (L x W x T) |
Format | Hardcover |
Pages | 1248 |
ISBN-13 | 978-0-471-21388-8 |
Barcode | 9780471213888 |
Categories | |
LSN | 0-471-21388-8 |