Ethical issues in studying the safety of approved drugs a letter report
The FDA requested that the IOM examine the ethical and informed consent issues that should be considered when conducting clinical trials to evaluate drug safety. This report outlines when and how the FDA should conduct clinical trials to protect the public's health and the health of trial parti...
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Format: | eBook |
Language: | English |
Published: |
Washington, D.C.
National Academies Press
2010, [2010]
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Online Access: | |
Collection: | National Center for Biotechnology Information - Collection details see MPG.ReNa |
Table of Contents:
- Includes bibliographical references