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Clinical Trials Handbook de SC Gad

Clinical Trials Handbook: Pharmaceutical Development Series

Autor SC Gad
en Limba Engleză Hardback – 20 iul 2009
Provides a comprehensive and thorough reference on the basics and practices of clinical trials Includes chapters on hot topics like: adverse event reporting (AER) systems, adaptive trial designs, and crossover trial designs Presents chapters on issues for specific disease areas: cardiology, oncology, cognitive, dermatology, etc.
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Specificații

ISBN-13: 9780471213888
ISBN-10: 0471213888
Pagini: 1248
Dimensiuni: 178 x 257 x 50 mm
Greutate: 2.12 kg
Editura: Wiley
Seria Pharmaceutical Development Series

Locul publicării:Hoboken, United States

Public țintă

Pharmaceutical scientists, technologists, toxicologists, biostatisticians, principal investigators, project managers, and IT specialists in clinical trial research, consultants and contract research organizations (CROs) involved in drug development research. Regulatory agency personnel in the US, EU, and Japan.

Notă biografică

Shayne Cox Gad, PhD, DABT, ATS, is the Principal of Gad Consulting Services. Dr. Gad has more than thirty years of experience as a toxicologist, statistical consultant, manager, and general consultant on research and development in the chemical, consumer product, contract testing, biotechnology, medical device, and pharmaceutical industries. He is the author of thirty-nine books and numerous papers, presentations, and other publications.

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