The role of the study director in nonclinical studies : pharmaceuticals, chemicals, medical devices, and pesticides / edited by William J. Brock, Brock Scientific Consulting, Montgomery Village, Maryland, USA ; associate editors, Barbara J. Mounho, ToxStrategies, Inc., Bend, Oregon, USA, Lijie Fu, SNBL, Beijing, China. [electronic resource] Brock, William J., editor of compilation. Mounho, Barbara J., editor of compilation. Fu, Lijie, 1953- editor of compilation. Medical laboratories Quality control. Biological laboratories Quality control. Health occupations schools. Allied health personnel In-service training. RB36.3.Q34 616.07/5 23 Includes index. Includes bibliographical references and index. Description based on print version record and CIP data provided by publisher. 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 studyCovers regulatory and scientific concepts, including international testing and Good Laboratory Practice (GLP), compliance with guidelines, an. 2014 Text 1 online resource. http://onlinelibrary.wiley.com/book/10.1002/9781118873922 eng Role of the study director in nonclinical studies Role of the study director in nonclinical studies