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Ethical Issues in International Research - 2009 (Session 7)

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Air date: Wednesday, November 4, 2009, 8:30:00 AM
Time displayed is Eastern Time, Washington DC Local
Views: Total views: 312 * This only includes stats from October 2011 and forward.
Category: Bioethics
Runtime: 02:24:58
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- 9:10                   Exploitation 

Alan Wertheimer PhD

                                    NIH Clinical Center Dept of Bioethics

 

9:10-9:20                    Discussion

 

9:20- 10:05                 Special issues in international research

                                    Joe Millum PhD

                                    NIH Clinical Center Dept of Bioethics

 

10:05-10:15                Discussion

 

10:15- 10:25               Break

 

10:25- 11:10               International research ethics: Informed consent and post trial considerations

Seema Shah JD

NIH Clinical Center Dept of Bioethics         

 

11:10- 11:20               Discussion

 

11:20- 11:30               Post tests and evaluations



For more information, visit
http://www.bioethics.nih.gov
NLM Title: Ethical issues in international research / Alan Wertheimer, Joe Millum, and Seema Shah.
Author: Wertheimer, Alan.
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. Alan Wertheimer PhD NIH Clinical Center Dept of Bioethics Joe Millum PhD NIH Clinical Center Dept of Bioethics Seema Shah JD Discussion Post tests and evaluations For more information, visit http://www.bioethics.nih.gov.
Subjects: Human Experimentation--ethics
International Cooperation
Research Subjects
Publication Types: Lecture
Webcast
NLM Classification: W 20.55.H9
NLM ID: 101520506
CIT Live ID: 7870
Permanent link: https://videocast.nih.gov/watch=7870

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