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IRB review, Conflicts of Interest and Investigator Perspectives - 2010 (Session 2)

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Air date: Wednesday, September 29, 2010, 8:30:00 AM
Time displayed is Eastern Time, Washington DC Local
Views: Total views: 71 * This only includes stats from October 2011 and forward.
Category: Bioethics
Runtime: 02:39:24
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 course. IRB review, conflicts of interest, and investigator perspectives [electronic resource] / Barbara Karp and Steve Joffe.
Series: IRB review, conflicts of interest, and investigator perspectives
Author: Karp, Barbara.
National Institutes of Health (U.S.)
Publisher:
Other Title(s): IRB review, conflicts of interest, and investigator perspectives
Abstract: (CIT): ECourse 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: Conflict of Interest
Ethics Committees, Research--ethics
Ethics, Research
Human Experimentation--ethics
Research Personnel--ethics
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: 101549172
CIT Live ID: 9624
Permanent link: https://videocast.nih.gov/launch.asp?16161

 

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