BEGIN:VCALENDAR VERSION:2.0 PRODID:VideoCast CALSCALE:GREGORIAN METHOD:PUBLISH BEGIN:VEVENT SUMMARY:Ethical & Regulatory Aspects of Clinical Research Session 5: Informed Consent, Research with Those with Impaired Capacity for Consent, and Research Ethics Consultation DTSTART:20191030T123000Z DTEND:20191030T153000Z DTSTAMP:20191031T132100Z UID:Videocast--34860 LOCATION:https://videocast.nih.gov/watch=34860 DESCRIPTION:Christine Grady\, RN\, PhD\, CC\, NIH\; Scott Kim\, MD\, PhD\, CC\, NIH and Marion Danis\, MD\, CC\, NIH\nThe Department of Bioethics offers this seven to eight 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.\n\nFor more information go to 'https://www.bioethics.nih.gov/courses/ethical-regulatory-aspects.shtml'>https://www.bioethics.nih.gov/courses/ethical-regulatory-aspects.shtml X-ALT-DESC;FMTTYPE=text/html:\n\n
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