{"product_id":"9780471213888","title":"Clinical Trials Handbook","description":"\u003ch3\u003ePharmaceutical Development Series\u003c\/h3\u003e\u003ch1\u003eClinical Trials Handbook\u003c\/h1\u003e\u003ch3\u003eShayne Cox Gad\u003c\/h3\u003e\u003cdiv\u003e\u003cb\u003eScience \/ Chemistry \/ Industrial \u0026amp; Technical\u003c\/b\u003e\u003c\/div\u003e\u003cbr\u003e\u003cdiv\u003e\n\u003cb\u003eBest practices for conducting effective and safe clinical trials\u003c\/b\u003e  \u003cp\u003eClinical 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. \u003ci\u003eClinical Trials Handbook\u003c\/i\u003e provides a comprehensive and thorough reference on the basics and practices of clinical trials.\u003c\/p\u003e \u003cp\u003eWith 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:\u003c\/p\u003e \u003cul\u003e \u003cli\u003eInterdisciplinary topics that have to be coordinated for a successful clinical trialData management (and adverse event reporting systems)\u003c\/li\u003e \u003cli\u003eBiostatistics, pharmacology, and toxicology\u003c\/li\u003e \u003cli\u003eModeling and simulation\u003c\/li\u003e \u003cli\u003eRegulatory monitoring and ethics\u003c\/li\u003e \u003cli\u003eParticular issues for given disease areas-cardiology, oncology, cognitive, dementia, dermatology, neuroscience, and more\u003c\/li\u003e \u003c\/ul\u003e With unique information on such current issues as adverse event reporting (AER) systems, adaptive trial designs, and crossover trial designs, \u003ci\u003eClinical Trials Handbook\u003c\/i\u003e will be a ready reference for pharmaceutical scientists, statisticians, researchers, and the many other professionals involved in drug development.\u003c\/div\u003e\u003cdiv\u003e \u003cb\u003eShayne Cox Gad, PhD, DABT, ATS\u003c\/b\u003e, is the Principal of Gad Consulting Services. Dr. Gad has more than thirty years of experience as a toxicologist, statistical consultant, manager, and general consultant on research and development in the chemical, consumer product, contract testing, biotechnology, medical device, and pharmaceutical industries. He is the author of thirty-nine books and numerous papers, presentations, and other publications.\u003c\/div\u003e\u003cbr\u003e\u003ctable\u003e\n\u003ctr\u003e\n\u003ctd\u003ePublication Date: \u003c\/td\u003e\n\u003ctd\u003e07 July 2009\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003ePublisher: \u003c\/td\u003e\n\u003ctd\u003eWiley\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eImprint: \u003c\/td\u003e\n\u003ctd\u003eWiley\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eISBN-13: \u003c\/td\u003e\n\u003ctd\u003e9780471213888\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eFormat: \u003c\/td\u003e\n\u003ctd\u003eHardback\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003ePage Count: \u003c\/td\u003e\n\u003ctd\u003e1248\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003eWeight (oz): \u003c\/td\u003e\n\u003ctd\u003e74.24\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003c\/table\u003e","brand":"Wiley","offers":[{"title":"Default Title","offer_id":44314359758988,"sku":"9780471213888","price":257.36,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0710\/9545\/1788\/files\/9780471213888_5ccccb1c-dc5e-4822-b711-e95137564c0b.jpg?v=1780155103","url":"https:\/\/fh90cf-fv.myshopify.com\/products\/9780471213888","provider":"Late Knight Books and Services, LLC","version":"1.0","type":"link"}