NIH VideoCast - Ethical and Regulatory Aspects of Clinical Research

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Air date:	Wednesday, November 14, 2007, 8:30:00 AM Time displayed is Eastern Time, Washington DC Local
Views:	Total views: 105 * This only includes stats from October 2011 and forward.
Category:	Bioethics
Runtime:	02:29:18
Closed captioning:	Check box to display CC outside of the video Note: You can drag the captioning window around and resize it
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. Genetics and stored tissue / Sara Chandros Hull, Gail Geller ; sponsored by the NIH Clinical Center [Dept.] of Bioethics.
Author:	Hull, Sara Chandros. National Institutes of Health (U.S.). Clinical Center. Department of Bioethics.
Publisher:
Subjects:	Conflict of Interest Ethics, Research Genetics--ethics Informed Consent--ethics Tissue Preservation--ethics
Publication Types:	Lecture Webcast
NLM Classification:	QU 450
NLM ID:	101322965
CIT Live ID:	6060
Permanent link:	https://videocast.nih.gov/watch=6060

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