History of and Framework for Human Subject Research and Conflicts of Interest (Session 1)

 


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Air date: Wednesday, September 26, 2007, 8:30:00 AM
Category: Bioethics
Runtime: 02:38:18
NLM Title: Ethical and regulatory aspects of clinical research. Session 1 [electronic resource] / Ezekiel Emanuel, Susan E. Lederer, and Cary Gross.
Author: Emanuel, Ezekiel J.
National Institutes of Health (U.S.). Clinical Center. Dept. of Bioethics.
Publisher: [Bethesda, Md. : National Institutes of Health, 2007]
Abstract: (CIT): Ethical and Regulatory Aspects of Clinical Research Department of Clinical Bioethics 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. Objectives of the Course: To learn the codes, declarations, and other documents that govern the ethical conduct of human subject research; review the critical elements of informed consent and their implementation in actual informed consent documents for clinical research; explore controversial issues relating to human subject research, including Phase I research, randomization, children in research, international research, etc; review the purpose if IRBs and provide IRB-like experience in reviewing research protocols; understand the experience of human subjects who have participated in research protocols. For more information, visit http://www.bioethics.nih.gov.
Subjects: Biomedical Research--ethics
Human Experimentation--ethics
Human Experimentation--history
Publication Types: Government Publications
Lectures
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NLM Classification: W 20.55.H9
NLM ID: 101317945
CIT File ID: 14042
CIT Live ID: 6053
Permanent link: http://videocast.nih.gov/launch.asp?14042

 

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