Edition: 1
Publisher:
Binding: Hardcover
ISBN / ASIN: 0471213888
Clinical Trials Handbook (Pharmaceutical Development Series)
Best practices for conducting effective and safe clinical trialsClinical trials are arguably the most important steps in proving drug effectiveness and safety for public use. Medical coding books Clinical Trials Handbook for free download collection in PDF, EPUB formats. 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. Ebooks download Clinical Trials Handbook pdf on amazon. Clinical Trials Handbook free download available via rapidshare, mediafire, 4shared, and hotfile.
Free Clinical Trials Handbook pdf
