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IRB review, Randomized Clinical Trials, and Research with Children

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Air date: Wednesday, October 8, 2014, 8:30:00 AM
Time displayed is Eastern Time, Washington DC Local
Views: Total views: 333, (65 Live, 268 On-demand)
Category: Bioethics
Runtime: 02:46:18
Description: Ethical and Regulatory Aspects of Clinical Research - Session 2

The 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, and is also available through Videocast. 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.

Purpose and Function of IRBs: Successes and Current Challenges
Richard Cannon MD Chair, NHLBI IRB

Ethics of Randomized Clinical Trials: Clinical Equipoise
Robert Truog MD Professor of Medical Ethics & Anaesthesia (Pediatrics) Harvard Medical School

Research with Children
Sara Goldkind MD
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NLM Title: Ethical and regulatory aspects of clinical research. Session 2, IRB review, randomized clinical trials, and research with children / Richard Cannon, Robert Truog.
Author: Cannon, Richard O.
Truog, Robert.
Goldkind, Sara F.
National Institutes of Health (U.S.),
Publisher:
Abstract: (CIT): Ethical and Regulatory Aspects of Clinical Research - Session 2 The 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, and is also available through Videocast. 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. Purpose and Function of IRBs: Successes and Current Challenges, Richard Cannon MD Chair, NHLBI IRB; Ethics of Randomized Clinical Trials: Clinical Equipoise, Robert Truog MD Professor of Medical Ethics & Anaesthesia (Pediatrics) Harvard Medical School; Research with Children, Sara Goldkind MD.
Subjects: Adolescent
Child
Ethics Committees, Research
Human Experimentation--ethics
Randomized Controlled Trials as Topic--ethics
Publication Types: Lecture
Webcasts
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Caption Text: Download Caption File
NLM Classification: W 20.55.E7
NLM ID: 101645883
CIT Live ID: 14699
Permanent link: https://videocast.nih.gov/launch.asp?18666