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The Role of the Study Director in Nonclinical Studies

Pharmaceuticals, Chemicals, Medical Devices, and Pesticides

Associate editor Barbara Mounho, Lijie Fu
Edited by William J. Brock
Format: Hardback
Publisher: John Wiley & Sons Inc, New York, United States
Published: 18th Jul 2014
Dimensions: w 226mm h 287mm d 38mm
Weight: 1538g
ISBN-10: 1118370392
ISBN-13: 9781118370391
Barcode No: 9781118370391
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Synopsis
A single-source reference with a broad and holistic overview of nonclinical studies, this book offers critical training material and describes regulations of nonclinical testing through guidelines, models, case studies, practical examples, and worldwide perspectives. The book: Provides a complete overview of nonclinical study organization, conduct, and reporting and describes the roles and responsibilities of a Study Director to manage an effective study Covers regulatory and scientific concepts, including international testing and Good Laboratory Practice (GLP), compliance with guidelines, and animal models Features a concluding chapter that compiles case studies / lessons learned from those that have served as a Study Director for many years Addresses the entire spectrum of nonclinical testing, making it applicable to those in the government, laboratories and those actively involved in in all sectors of industry

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