IUB Library OPAC
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.
Material type:
TextPublisher: Hoboken, New Jersey : John Wiley & Sons, [2014]Description: 1 online resourceContent type: text Media type: computer Carrier type: online resourceISBN: 9781118874080 (epub); 1118874080 (epub); 9781118873908 (pdf); 1118873904 (pdf); 9781118873922; 1118873920; 1118370392; 9781118370391Subject(s): Medical laboratories -- Quality control | Biological laboratories -- Quality control | Health occupations schools | Allied health personnel -- In-service training | HEALTH & FITNESS -- Diseases -- General | MEDICAL -- Clinical Medicine | MEDICAL -- Diseases | MEDICAL -- Evidence-Based Medicine | MEDICAL -- Internal Medicine | Allied health personnel -- In-service training | Biological laboratories -- Quality control | Health occupations schools | Medical laboratories -- Quality controlGenre/Form: Electronic books. | Electronic books.Additional physical formats: Print version:: Role of the study director in nonclinical studiesDDC classification: 616.07/5 LOC classification: RB36.3.Q34Online resources: Wiley Online Library Summary: 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.
Includes index.
Description based on print version record and CIP data provided by publisher.
Includes bibliographical references and index.
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.