Author:
Edition: 1
Publisher: The Johns Hopkins University Press
Binding: Paperback
ISBN: 0801878136
Ethical and Regulatory Aspects of Clinical Research: Readings and Commentary
All investigators funded by the National Institutes of Health are now required to receive training about the ethics of clinical research. Medical books Ethical and Regulatory Aspects 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 Medical books Ethical And Regulatory Aspects Of Clinical Research: Readings And Commentary, ,. payment | shipping rates | returns Ethical and Regulatory Aspects of Clinical Research: Readings and Commentary Product Category :Books ISBN :0801878136 Title :Ethical and Regulatory Aspects of Clinical Research: Readings and Commentary EAN :9780801878138 Binding :Paperback Publisher :The Johns Hopkins University Pre Publication Date :2003-09-30 Pages :528 Signed :False First Edition :False Dust Jacket :False List Price (MSRP) :47.00 Height :1.2400 inches Width :8.5200 inches Length :10.9200 in
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Medical Book Ethical and Regulatory Aspects 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.