NIH VideoCast - Ethical & Regulatory Aspects of Clinical Research Session 2: Randomized Clinical Trials/Risk-Benefit/Institutional Review Boards

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Ethical & Regulatory Aspects of Clinical Research Session 2: Randomized Clinical Trials/Risk-Benefit/Institutional Review Boards

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Air date:	Wednesday, September 29, 2021, 8:30:00 AM Time displayed is Eastern Time, Washington DC Local
Views:	Total views: 1,240 (433 Live, 807 On-demand)
Category:	Bioethics
Runtime:	02:41:09
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

NLM Title:	Ethical & regulatory aspects of clinical research. Session 2, Randomized clinical trials/Risk-Benefit/Institutional review boards / Robert Truog, David Wendler, Holly Taylor.
Author:	Truog, Robert. Wendler, David. Taylor, Holly. National Institutes of Health (U.S.), National Institutes of Health (U.S.). Clinical Center. Department of Bioethics,
Publisher:
Abstract:	(CIT): 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.
Subjects:	Ethics Committees, Research--ethics Ethics, Research Human Experimentation--ethics Randomized Controlled Trials as Topic--ethics Risk Assessment
Publication Types:	Lecture Webcast

NLM Classification:	W 20.55.H9
NLM ID:	9918282191106676
CIT Live ID:	42671
Permanent link:	https://videocast.nih.gov/watch=42671

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