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History, Guidance, and Framework for Ethical Clinical Research - 2010 (Session 1)

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Air date: Wednesday, September 22, 2010, 8:30:00 AM
Time displayed is Eastern Time, Washington DC Local
Views: Total views: 376 * This only includes stats from October 2011 and forward.
Category: Bioethics
Runtime: 02:47:16
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. History, guidance, and framework for ethical clinical research [electronic resource] / Christine Grady, Susan E. Lederer, and Heidi Gertner.
Series: History, guidance, and framework for ethical clinical research
Author: Grady, Christine.
National Institutes of Health (U.S.)
Publisher:
Other Title(s): History, guidance, and framework for ethical clinical research
Subjects: Human Experimentation--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: 101546236
CIT Live ID: 9623
Permanent link: https://videocast.nih.gov/launch.asp?16144

 

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