NIH VideoCast - Ethical & Regulatory Aspects of Clinical Research Session 1: Ethical Framework/ Risk Benefit Assessment

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Ethical & Regulatory Aspects of Clinical Research Session 1: Ethical Framework/ Risk Benefit Assessment

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Air date:	Wednesday, September 23, 2020, 8:30:00 AM Time displayed is Eastern Time, Washington DC Local
Views:	Total views: 2,197 (877 Live, 1,320 On-demand)
Category:	Bioethics
Runtime:	02:43:00
Closed captioning:	Check box to display CC outside of the video Note: You can drag the captioning window around and resize it
Description:	The Department of Bioethics offers this seven week course annually each fall. The course is designed to provide an overview of the important issues in the ethics of human subject research for clinical investigators and others who participate in the conduct of research and is open to the entire NIH community as well as to those from outside NIH. Topics include the history of human subject research ethics, principles and guidelines, study design, subject recruitment, informed consent, and international research. The course is open to the entire NIH community as well as to those from outside NIH. The recommended textbook is Ethical and Regulatory Aspects of Clinical Research, edited by Emanuel et al (Johns Hopkins University Press). The course is taught by guest faculty and faculty members from the National Institutes of Health. This is a required academic program for Bioethics fellows. For more information go to https://www.bioethics.nih.gov/courses/ethical-regulatory-aspects.shtml

Author:	Christine Grady, RN, PhD, NIH, Holly Taylor, PhD, MPH, NIH and David Wendler, PhD, NIH

CIT Live ID:	38645
Permanent link:	https://videocast.nih.gov/watch=38645

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