Risks and Benefits; Special Populations in Research - 2008 (Session 5)

 


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Air date: Wednesday, October 22, 2008, 8:30:00 AM
Category: Bioethics
Runtime: 180 minutes
NLM Title: Ethical and regulatory aspects of clinical research. Session 5, Risks and benefits and impaired decision making [electronic resource] / Dave Wendler ... [et al.] ; sponsored by NIH Clinical Center, Department of Bioethics.
Series: Risks and benefits, special populations in research, 2008 (session 5)
Author: Wendler, David.
National Institutes of Health (U.S.). Clinical Center. Dept. of Bioethics.
Publisher: [Bethesda, Md. : National Institutes of Health, 2008]
Other Title(s): Risks and benefits, special populations in research, 2008 (session 5)
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
Decision Making--ethics
Mental Competency
Risk Assessment
Publication Types: Government Publications
Lectures
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NLM Classification: W 20.5
NLM ID: 101488643
CIT File ID: 14713
CIT Live ID: 7157
Permanent link: http://videocast.nih.gov/launch.asp?14713

 

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