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Ethical and Regulatory Aspects of Clinical Research: Readings and Commentary

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Click here to buy Ethical and Regulatory Aspects of Clinical Research: Readings and Commentary by  Ezekiel J. Emanuel, Robert A. Crouch, John D. Arras, and Jonathan D. Moreno. Ethical and Regulatory Aspects of Clinical Research: Readings and Commentary
by Ezekiel J. Emanuel, Robert A. Crouch, John D. Arras, and Jonathan D. Moreno
Sales Rank: 35340
5.0 out of 5 stars
$33.70
At Amazon
on 9-27-2008.
Buy Ethical and Regulatory Aspects of Clinical Research: Readings and Commentary now! Get Info on Ethical and Regulatory Aspects of Clinical Research: Readings and Commentary
Features
  • Cover Type: Paperback with 528 pages
  • Published by: The Johns Hopkins University Press
  • Edition: 1st Edition September 30, 2003
  • Written in: English
  • ISBN 10 Number: 0801878136
  • ISBN 13 Number: 978-0801878138
  • Book Dimensions: 10.9 x 8.5 x 1.2 inches
  • Weighs: 3.2 pounds

Product Review


"Provides great material on a broad variety of ethical topics in clinical research. The editors are commended for the wise and diverse selection of articles and the broad range of sources of literature included. A lot of information is made available at a very affordable price." -- Quality Assurance Journal



"Many of the chapters easily deserve to be required reading Most of the readings that have been chosen for the book can lay claim to being classics. They represent sophisticated thinking on various topics." -- Leonardo D. de Castro, Bulletin of the World Health Organization



"One word will suffice to describe the book -- outstanding." -- Sanjay A. Pai, Current Science

Product Description


All investigators funded by the National Institutes of Health are now required to receive training about the ethics of clinical research. Based on a course taught by the editors at NIH, Ethical and Regulatory Aspects of Clinical Research is the first book designed to help investigators meet this new requirement. The book begins with the history of human subjects research and guidelines instituted since World War II. It then covers various stages and components of the clinical trial process: designing the trial, recruiting participants, ensuring informed consent, studying special populations, and conducting international research. Concluding chapters address conflicts of interest, scientific misconduct, and challenges to the IRB system. The appendix provides sample informed consent forms.

This book will be used in undergraduate courses on research ethics and in schools of medicine and public health by students who are or will be carrying out clinical research. Professionals in need of such training and bioethicists also will be interested.

Reader Reviews
This book is a great resource and reference. It's a great collection of short articles useful for those interested in the ethical issues surrounding research. It has full copies of the Nuremberg and other ethical codes.


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Ethical and Regulatory Aspects of Clinical Research: Readings and Commentary
List Price: $41.00
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Price: $33.70
Updated on 9-27-2008.
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