Ethical and Regulatory Aspects of Clinical Research: Readings and Commentary

Book details

Details for Ethical and Regulatory Aspects of Clinical Research: Readings and Commentary
AuthorCrouch, Robert A.,Arras, John D.,Ezekiel J. Emanuel,Jonathan D. Moreno,Grady, Christine
PublisherJohns Hopkins University Press
Bindingpaperback
PublishedSeptember 30, 2003
EditionIllustrated
LanguageEnglish
Pages528
ISBN-100801878136
ISBN-139780801878138
Weight3.35 lb
Dimensions
H × W × L
1.42 in × 8.54 in × 10.98 in

Ethical and Regulatory Aspects of Clinical Research: Readings and Commentary

$29.24 $50.00
Availability:
In stock
SKU:
0801878136-5
Condition
Condition notes

Used book in acceptable condition. Pages and cover may have wear, tears, or stickers. Notes or highlighting are possible. CDs and access codes may be missing.

About this book

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...

Read the full 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.


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