Author: J. Rick Turner PhD
Edition:
Publisher: Turner Medical Communications LLC
Binding: Paperback
ISBN: 0615507670
A Concise Guide to Clinical Trials
Biopharmaceutical drugs improve the health and well-being of people across the globe on a scale that is unrivaled by any other medical intervention. Medical books A Concise Guide to Clinical Trials. Before these drugs can be prescribed for patients by their doctors, they have to be approved for marketing by a regulatory agency. To gain marketing approval, drugs must go through an extremely rigorous process that investigates their safety and efficacy, the process of New Drug Development. The last stage of this long, complex, and expensive process involves conducting clinical trials, the topic of this book. Successfully conducting clinical trials requires the interdisciplinary collaboration of individuals from many clinical and scientific disciplines and areas of operational expertise Medical books A Concise Guide To Clinical Trials Ebook. Buy A Concise Guide to Clinical Trials by Allan Hackshaw and Read this Book on Kobo's Free Apps. Discover Kobo's Vast Collection of Ebooks Today - Over 3 Million Titles, Including 2 Million Free Ones!
Download link for A Concise Guide to Clinical Trials
Buy A Concise Guide to Clinical Trials by Allan Hackshaw and Read this Book on Kobo's Free Apps. Discover Kobo's Vast Collection of Ebooks Today - Over 3 Million Titles, Including 2 Million Free Ones!
A Concise Guide to Clinical Trials, ISBN-13: 9780615507675, ISBN-10: 0615507670
A Concise Guide to Clinical Trials
Store Search search Title, ISBN and Author A Concise Guide to Clinical Trials by Elizabeth Paul, Allan Hackshaw Estimated delivery 3-12 business days Format Paperback Condition Brand New Finally, a concise guide to setting up, conducting, and reporting a clinical trial. Covering the scientific basis of the design and analyses of clinical trials, including the statistical issues and how they are coordinated and regulated, this important paperback illuminates the path to success for the student o
Medical Book A Concise Guide to Clinical Trials
Before these drugs can be prescribed for patients by their doctors, they have to be approved for marketing by a regulatory agency. To gain marketing approval, drugs must go through an extremely rigorous process that investigates their safety and efficacy, the process of New Drug Development. The last stage of this long, complex, and expensive process involves conducting clinical trials, the topic of this book. Successfully conducting clinical trials requires the interdisciplinary collaboration of individuals from many clinical and scientific disciplines and areas of operational expertise. These include medicine, information technology, ethics and law, statistics, clinical trial operations, data collection and management, regulatory science, and medical writing, to name just a few. Central aspects of conducting clinical trials are discussed in the following chapters, with the goals of making specialists from each of these areas aware of the contributions of their colleagues, and helping readers to appreciate that everyone involved in clinical research is working side-by-side toward a common goal---improving the health, well-being, and longevity of millions of patients around the globe.
