Description

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.

More Details about Clinical Trials Handbook (HB)

General Information  
Author(s)Gad
PublisherJohn Wiley
ISBN9780471213888
Pages1225
BindingHard Back
LanguageEnglish
Publish YearJanuary 2009