NIH VideoCast - Informed Consent

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Air date:	Wednesday, October 29, 2008, 8:30:00 AM Time displayed is Eastern Time, Washington DC Local
Views:	Total views: 137 * This only includes stats from October 2011 and forward.
Category:	Bioethics
Runtime:	02:40:18
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. Session 6, Informed consent, 2008 / [speaker, Seema Shah].
Author:	Shah, Seema.
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:	Ethics, Research Informed Consent--legislation & jurisprudence
Publication Types:	Lecture Webcast
NLM Classification:	W 32.6
NLM ID:	101488658
CIT Live ID:	7159
Permanent link:	https://videocast.nih.gov/watch=7159

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