Ethical Issues in International Research - 2009 (Session 7) |
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| Air date: | Wednesday, November 04, 2009, 8:30:00 AM Time displayed is Eastern Time, Washington DC Local |
| Category: | Bioethics |
| 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 Joe
Millum PhD NIH Clinical
Center Dept of Bioethics 10:05-10:15 Discussion 10:15- Seema Shah
JD NIH
Clinical Center Dept of Bioethics
For more information, visit http://www.bioethics.nih.gov |
| Author: | Alan Wertheimer, Joe Millum and Seema Shah |
| Runtime: | 180 minutes |
| Download: | Download
Video How to download a Videocast |
| CIT File ID: | 15416 |
| CIT Live ID: | 7870 |
| Permanent link: | http://videocast.nih.gov/launch.asp?15416 |
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Enhanced Audio Podcast | 2:24:58 |
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Enhanced Video Podcast | 2:24:58 | |