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Description
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 authors, the book takes the reader through each trial phase, technique, and issue. Chapters cover every key aspect of preparing and conducting clinical trials, including: Interdisciplinary topics that have to be coordinated for a successful clinical trialData management (and adverse event reporting systems) Biostatistics, pharmacology, and toxicology Modeling and simulation Regulatory monitoring and ethics Particular issues for given disease areas-cardiology, oncology, cognitive, dementia, dermatology, neuroscience, and more With unique information on such current issues as adverse event reporting (AER) systems, adaptive trial designs, and crossover trial designs, Clinical Trials Handbook will be a ready reference for pharmaceutical scientists, statisticians, researchers, and the many other professionals involved in drug development.
Pages
1248 pages
Collection
Pharmaceutical Development Series
Parution
2009-06-17
Marque
Wiley
EAN papier
9780471213888
EAN PDF
9780470466353
Informations sur l'ebook
Nombre pages copiables
0
Nombre pages imprimables
1248
Taille du fichier
7608 Ko
Ce livre est accessible aux handicaps Voir les informations sur l'accessibilité
Prix
255,26 €

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