Informed Consent - 2008 (Session 6) |
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| Launch in standalone player | |
| Air date: | Wednesday, October 29, 2008, 8:30:00 AM |
| Category: | Bioethics |
| Runtime: | 180 minutes |
| NLM Title: | Ethical and regulatory aspects of clinical research. Session 6, Informed consent, 2008 [electronic resource] / [speaker, Seema Shah]. |
| Series: | Informed consent |
| Author: | Shah, Seema. |
| Publisher: | [Bethesda, Md. : National Institutes of Health, 2008] |
| Other Title(s): | Informed consent |
| 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. For more information, visit http://www.bioethics.nih.gov. |
| Subjects: | Ethics, Research Informed Consent--legislation & jurisprudence |
| Publication Types: | Government Publications Lectures |
| Download: | Download
Video How to download a Videocast |
| NLM Classification: | W 32.6 |
| NLM ID: | 101488658 |
| CIT File ID: | 14731 |
| CIT Live ID: | 7159 |
| Permanent link: | http://videocast.nih.gov/launch.asp?14731 |
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Enhanced Audio Podcast | 2:40:18 |
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Enhanced Video Podcast | 2:40:18 | |