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Informed Consent and Special Populations - 2010 (Session 7)

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Air date: Wednesday, November 3, 2010, 8:30:00 AM
Time displayed is Eastern Time, Washington DC Local
Views: Total views: 179 * This only includes stats from October 2011 and forward.
Category: Bioethics
Runtime: 02:37:59
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, Informed consent and special populations, 2010 [electronic resource] / Christine Grady, Don Rosenstein, and Maggie Little.
Author: Grady, Christine.
National Institutes of Health (U.S.)
Publisher:
Abstract: (CIT): 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.
Subjects: Biomedical Research
Human Experimentation
Informed Consent
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: 101549239
CIT Live ID: 9629
Permanent link: https://videocast.nih.gov/launch.asp?16248

 

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