Del 8 - Pharmaceutical Development Series
Clinical Trials Handbook
Inbunden, Engelska, 2009
Av Shayne Cox Gad, North Carolina) Gad, Shayne Cox (IBS, Raleigh
3 669 kr
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Fri frakt för medlemmar vid köp för minst 249 kr.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 toxicologyModeling and simulationRegulatory monitoring and ethicsParticular issues for given disease areas-cardiology, oncology, cognitive, dementia, dermatology, neuroscience, and moreWith 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.
Produktinformation
- Utgivningsdatum2009-07-21
- Mått186 x 260 x 50 mm
- Vikt2 105 g
- FormatInbunden
- SpråkEngelska
- SeriePharmaceutical Development Series
- Antal sidor1 248
- FörlagJohn Wiley & Sons Inc
- ISBN9780471213888