[PDF.34su] Clinical Trials, Second Edition: Study Design, Endpoints and Biomarkers, Drug Safety, and FDA and ICH Guidelines

Clinical Trials, Second Edition: Study Design, Endpoints and Biomarkers, Drug Safety, and FDA and ICH Guidelines

[PDF.oq68] Clinical Trials, Second Edition: Study Design, Endpoints and Biomarkers, Drug Safety, and FDA and ICH Guidelines

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 | #422594 in Books |  ACADEMIC PRESS |  2016-03-26 | Original language:English | PDF # 1 |  9.25 x1.88 x7.52l,3.90 | File type: PDF | 896 pages

 | ACADEMIC PRESS

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||2 of 2 people found the following review helpful.| Great Reference for Those Working in Industry|By Scriptor|I would strongly recommend this book for those beginning a career in the pharmaceutical industry or for those already working in industry for use as a reference. It is especially useful in the oncology therapeutic area and for its explanations of frequently-used statistical analyses. It is thorough, broad in scope, and w|About the Author|Dr. Tom Brody received his PhD from the University of California at Berkeley in 1980, and conducted postdoctoral research at University of Wisconsin-Madison and also at U.C. Berkeley. His 20 research publications concern the metabolism and pharm

Clinical Trials, Second Edition, offers those engaged in clinical trial design a valuable and practical guide. This book takes an integrated approach to incorporate biomedical science, laboratory data of human study, endpoint specification, legal and regulatory aspects and much more with the fundamentals of clinical trial design. It provides an overview of the design options along with the specific details of trial design and offers guidance on how to make ...

You can specify the type of files you want, for your device.Clinical Trials, Second Edition: Study Design, Endpoints and Biomarkers, Drug Safety, and FDA and ICH Guidelines   |  Tom Brody PhD. Just read it with an open mind because none of us really know.

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