Kód: 01389374
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 i ... celý popis
321.44 €
Potrebujete viac kusov?Ak máte záujem o viac kusov, preverte, prosím, najprv dostupnosť titulu na našej zákazníckej podpore.
Nákupom získate 796 bodov
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.Best practices for conductingeffective 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.
Zaradenie knihy Knihy po anglicky Technology, engineering, agriculture Industrial chemistry & manufacturing technologies Industrial chemistry
321.44 €
Osobný odber Bratislava a 2642 dalších
Copyright ©2008-24 najlacnejsie-knihy.sk Všetky práva vyhradenéSúkromieCookies
Nákupný košík ( prázdny )