NIH VideoCast - RCTs, Placebo, Stored Tissue

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Air date:	Wednesday, October 6, 2010, 8:30:00 AM Time displayed is Eastern Time, Washington DC Local
Views:	Total views: 123 * This only includes stats from October 2011 and forward.
Category:	Bioethics
Runtime:	02:42:49
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. Session 3, RCTs, placebo, stored tissue / Sara Chandros Hull, Robert Truog, and Frank Miller.
Author:	Hull, Sara Chandros. National Institutes of Health (U.S.)
Publisher:
Abstract:	(CIT): 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:	Ethics, Research Randomized Controlled Trials as Topic--ethics Research Design Tissue Banks--ethics Tissue Preservation--ethics
Publication Types:	Lecture Webcast
NLM Classification:	QS 523
NLM ID:	101549188
CIT Live ID:	9625
Permanent link:	https://videocast.nih.gov/watch=9625

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