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Ethical and Regulatory Aspects of Clinical Research Course 6

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Air date: Wednesday, December 10, 2003, 8:30:00 AM
Time displayed is Eastern Time, Washington DC Local
Views: Total views: 108 * This only includes stats from October 2011 and forward.
Category: Bioethics
Runtime: 02:37:48
Description: Practical Aspects of Informed Consent
Alison Wichman, MD
Deputy Director, Office of Human Subject Research
Office of the Director, NIH

Informed Consent: What do the Data Show?

Research Involving Persons at Risk for Impaired Decision-Making
Donald Rosenstein, MD
Chief, Psychiatry Consult-Liaison Service
Deputy Clinical Director, NIMH

This course is designed to provide a historical context for research regulations and to help researchers and others working in human subject research gain insights and skills into the development of research protocols and their ethical implementation.
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NLM Title: Ethical and regulatory aspects of clinical research. Course 6 / [Alison Wichman, Christine Grady, Donald Rosenstein].
Author: Wichman, Alison.
National Institutes of Health (U.S.)
Abstract: (CIT): Practical Aspects of Informed Consent, Alison Wichman, MD, Deputy Director, Office of Human Subject Research, Office of the Director, NIH. Informed Consent: What do the Data Show? Research Involving Persons at Risk for Impaired Decision-Making, Donald Rosenstein, MD, Chief, Psychiatry Consult-Liaison Service, Deputy Clinical Director, NIMH.
Subjects: Biomedical Research--ethics
Decision Making
Informed Consent--ethics
Informed Consent--standards
Research Subjects
Vulnerable Populations
Publication Types: Lecture
Rights: This is a work of the United States Government. No copyright exists on this material. It may be disseminated freely.
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NLM Classification: W 20.5
NLM ID: 101268312
CIT Live ID: 2677
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