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Risks and Benefits - 2009 (Session 5)

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Air date: Wednesday, October 21, 2009, 8:30:00 AM
Time displayed is Eastern Time, Washington DC Local
Views: Total views: 146 * This only includes stats from October 2011 and forward.
Category: Bioethics
Runtime: 02:46:41
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.

8:30-9:15                    Assessment of Risks and Benefits

                                    Dave Wendler PhD

                                    NIH Clinical Center Dept of Bioethics

             

9:15-9:25                    Discussion

 

9:25-10:10                  Ethical Issues in the Use of Stored Tissue and Data

Sara Chandros Hull, Ph.D.

NHGRI and Dept of Bioethics

 

10:10-10:20                Discussion

 

10:20-10:35                Break

 

10:35- 11:30              Investigator Panel

                                                Crystal Mackall MD (pediatrics)

                                                Jorge Tavel MD  (HIV/ international/ flu vaccine)

                                                Tito Fojo MD  (medical oncology)

For more information, visit
http://www.bioethics.nih.gov

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NLM Title: Risks and benefits / Dave Wendler ... [et al.].
Author: Wendler, David.
National Institutes of Health (U.S.). Clinical Center.
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. Assessment of Risks and Benefits (medical oncology)
Subjects: Ethics, Research
Human Experimentation--ethics
Risk Assessment
Publication Types: Lectures
Webcasts
Download: To download this event, select one of the available bitrates:
[384k]    How to download a Videocast
NLM Classification: W 20.55.H9
NLM ID: 101518988
CIT Live ID: 7868
Permanent link: https://videocast.nih.gov/launch.asp?15375

 

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