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

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Air date: Wednesday, October 22, 2008, 8:30:00 AM
Time displayed is Eastern Time, Washington DC Local
Views: Total views: 116 * This only includes stats from October 2011 and forward.
Category: Bioethics
Runtime: 02:42:52
Description: 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
NLM Title: Ethical and regulatory aspects of clinical research. Session 5, Risks and benefits and impaired decision making / Dave Wendler ... [et al.] ; sponsored by NIH Clinical Center, Department of Bioethics.
Author: Wendler, David.
National Institutes of Health (U.S.). Clinical Center. Department of Bioethics.
Publisher:
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: Lecture
Webcast
NLM Classification: W 20.5
NLM ID: 101488643
CIT Live ID: 7157
Permanent link: https://videocast.nih.gov/watch=7157

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