NIH VideoCast - Ethical & Regulatory Aspects of Clinical Research Session 4: Informed Consent/Decision Making/Capacity Assessment

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Ethical & Regulatory Aspects of Clinical Research Session 4: Informed Consent/Decision Making/Capacity Assessment

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Air date:	Wednesday, October 13, 2021, 8:30:00 AM Time displayed is Eastern Time, Washington DC Local
Views:	Total views: 796 (363 Live, 433 On-demand)
Category:	Bioethics
Runtime:	02:42:40
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 4, Informed consent/decision making/capacity assessment / Christine Grady, Scott Kim, Katherine Todman, Holly Taylor.
Author:	Grady, Christine. Kim, Scott Y H. Todman, Katherine. Taylor, Holly. 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:	Decision Making--ethics Human Experimentation--ethics Informed Consent--ethics
Publication Types:	Lecture Webcast

NLM Classification:	W 20.55.H9
NLM ID:	9918299485006676
CIT Live ID:	42675
Permanent link:	https://videocast.nih.gov/watch=42675

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