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Codes, IRB Review and Ethical Issues in Study Design (Session 2)

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Air date: Wednesday, October 3, 2007, 8:30:00 AM
Time displayed is Eastern Time, Washington DC Local
Views: Total views: 169 * This only includes stats from October 2011 and forward.
Category: Bioethics
Runtime: 02:41:05
Description: Ethical and Regulatory Aspects of Clinical Research

Department of Clinical Bioethics

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.

For more information, visit
http://www.bioethics.nih.gov
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NLM Title: Codes, IRB review and ethical issues in study design / Christine Grady, Jerry Menikoff, and Frank Miller.
Author: Grady, Christine.
National Institutes of Health (U.S.)
Publisher:
Abstract: (CIT): Ethical and Regulatory Aspects of Clinical Research Department of Clinical Bioethics 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: Ethics Committees, Research--ethics
Human Experimentation--ethics
Research Design
Publication Types: Lecture
Webcasts
Download: To download this event, select one of the available bitrates:
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NLM Classification: W 20.55.H9
NLM ID: 101319927
CIT Live ID: 6054
Permanent link: https://videocast.nih.gov/launch.asp?14056