NIH VideoCast - Ethical & Regulatory Aspects of Clinical Research Session 1: Ethical Framework/Physician-Investigator Role/History of Research Ethics

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Ethical & Regulatory Aspects of Clinical Research Session 1: Ethical Framework/Physician-Investigator Role/History of Research Ethics

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Air date:	Wednesday, September 22, 2021, 8:30:00 AM Time displayed is Eastern Time, Washington DC Local
Views:	Total views: 1,467 (518 Live, 949 On-demand)
Category:	Bioethics
Runtime:	02:50:50
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 1, Ethical framework/physician-investigator role/history of research ethics / Holly Taylor, Christine Grady, Steven Joffe.
Author:	Taylor, Holly. Grady, Christine. Joffe, Steven. 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, Research Human Experimentation--ethics Physician-Patient Relations--ethics Research Design Research--legislation & jurisprudence Researcher-Subject Relations--ethics
Publication Types:	Lecture Webcast

NLM Classification:	W 20.55.E7
NLM ID:	9918282192606676
CIT Live ID:	42669
Permanent link:	https://videocast.nih.gov/watch=42669

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