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Clinical trials handbook /

Best practices for conducting effective and safe clinical trials. 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, p...

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Detalles Bibliográficos
Clasificación:Libro Electrónico
Otros Autores: Gad, Shayne C., 1948-
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Hoboken, NJ : Wiley, ©2009.
Colección:Pharmaceutical Development Series.
Temas:
Acceso en línea:Texto completo
Descripción
Sumario:Best practices for conducting effective and safe clinical trials. 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 au.
Descripción Física:1 online resource (xix, 1225 pages) : illustrations.
Bibliografía:Includes bibliographical references and index.
ISBN:9780471213888
0471213888
9780470466353
0470466359
1282368443
9781282368446
9786612368448
6612368446
0470466367
9780470466360