NIH VideoCast - Informed Consent and Special Populations

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Air date:	Wednesday, November 3, 2010, 8:30:00 AM Time displayed is Eastern Time, Washington DC Local
Views:	Total views: 298 * This only includes stats from October 2011 and forward.
Category:	Bioethics
Runtime:	02:37:59
Closed captioning:	Check box to display CC outside of the video Note: You can drag the captioning window around and resize it
Description:	Ethical and Regulatory Aspects of Clinical Research Course Objectives By the end of this course, participants will be able to: Utilize a systematic framework for evaluating the ethics of a clinical research protocol. Apply appropriate codes, regulations, and other documents governing the ethical conduct of human subject research to their own research. Discuss controversial issues relating to human subject research, including Phase 1 research, randomization, children in research, international research, etc. Identify the critical elements of informed consent and strategies for implementing informed consent for clinical research. Describe the purpose, function, and challenges of IRBs. Appreciate the experience of human subjects who have participated in research protocols. For more information, visit http://www.bioethics.nih.gov/hsrc/index.shtml

NLM Title:	Ethical and regulatory aspects of clinical research, Informed consent and special populations, 2010 / Christine Grady, Don Rosenstein, and Maggie Little.
Author:	Grady, Christine. National Institutes of Health (U.S.)
Publisher:
Abstract:	(CIT): Ethical and Regulatory Aspects of Clinical Research Course Objectives By the end of this course, participants will be able to: Utilize a systematic framework for evaluating the ethics of a clinical research protocol. Apply appropriate codes, regulations, and other documents governing the ethical conduct of human subject research to their own research. Discuss controversial issues relating to human subject research, including Phase 1 research, randomization, children in research, international research, etc. Identify the critical elements of informed consent and strategies for implementing informed consent for clinical research. Describe the purpose, function, and challenges of IRBs. Appreciate the experience of human subjects who have participated in research protocols.
Subjects:	Biomedical Research Human Experimentation Informed Consent
Publication Types:	Lecture Webcast
NLM Classification:	W 20.55.H9
NLM ID:	101549239
CIT Live ID:	9629
Permanent link:	https://videocast.nih.gov/watch=9629

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