History, Guidance, and Framework for Ethical Clinical Research - 2008 (Session 1)

 


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Air date: Wednesday, September 24, 2008, 8:30:00 AM
Category: Bioethics
Runtime: 180 minutes
NLM Title: Ethical and regulatory aspects of clinical research. Session 1, History, guidance, and framework for ethical clinical research [electronic resource] / Ezekiel Emanuel, Susan E. Lederer, and Christine Grady.
Series: History, guidance, and framework for ethical clinical research
Author: Emanuel, Ezekiel J.
National Institutes of Health (U.S.)
Publisher: [Bethesda, Md. : National Institutes of Health, 2008]
Other Title(s): History, guidance, and framework for ethical clinical research
Abstract: (CIT): This course is designed to provide a historical context for research regulations and to help researchers and others working in human subject research gain insights and skills into the development of research protocols and their ethical implementation. Objectives of the Course: To learn the codes, declarations, and other documents that govern the ethical conduct of human subject research; review the critical elements of informed consent and their implementation in actual informed consent documents for clinical research; explore controversial issues relating to human subject research, including Phase I research, randomization, children in research, international research, etc; review the purpose if IRBs and provide IRB-like experience in reviewing research protocols; understand the experience of human subjects who have participated in research protocols.
Subjects: Biomedical Research--ethics
Ethics, Research--history
Guidelines as Topic
Human Experimentation--ethics
Human Experimentation--history
Publication Types: Government Publications
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NLM Classification: W 20.5
NLM ID: 101486646
CIT File ID: 14664
CIT Live ID: 7153
Permanent link: http://videocast.nih.gov/launch.asp?14664

 

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