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Fair Subject Selection & Recruitment, Undue Influence and Coercion - 2010 (Session 4)

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Air date: Wednesday, October 13, 2010, 8:30:00 AM
Time displayed is Eastern Time, Washington DC Local
Views: Total views: 95 * This only includes stats from October 2011 and forward.
Category: Bioethics
Runtime: 02:52:27
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
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NLM Title: Ethical and regulatory aspects of clinical research. Fair subject selection & recruitment, undue influence and coercion-2010 [electronic resource] / Dave Wendler and Alan Wertheimer.
Series: Fair subject selection & recruitment, undue influence, and coercion
Author: Wendler, David.
National Institutes of Health (U.S.)
Publisher:
Other Title(s): Fair subject selection & recruitment, undue influence, and coercion
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: Coercion
Ethics, Research
Human Experimentation--ethics
Patient Selection--ethics
Research Subjects
Publication Types: Lectures
Webcasts
Download: To download this event, select one of the available bitrates:
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NLM Classification: W 20.55.H9
NLM ID: 101549192
CIT Live ID: 9626
Permanent link: https://videocast.nih.gov/launch.asp?16194

 

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