| Title: |
Ethical and regulatory aspects of clinical research. Session 1 [electronic resource] / Ezekiel Emanuel, Susan E. Lederer, and Cary Gross. |
| Author(s)/Name(s): |
Emanuel, Ezekiel J., |
| Publisher: |
[Bethesda, Md. : National Institutes of Health, 2007] |
| Related Names: |
National Institutes of Health (U.S.). Clinical Center. Dept. of Bioethics. |
| Language: |
eng |
| Electronic Links: |
http://videocast.nih.gov/launch.asp?14042 |
| MeSH Subjects: |
Human Experimentation --ethics |
|
Biomedical Research --ethics |
|
Human Experimentation --history |
|
Lectures |
| Summary: |
(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. |
| Notes: |
Title from title screen (viewed Oct. 29, 2007). |
|
Streaming video (2 hr., 38 min., 19 sec. : sd., col.). |
|
Mode of access: World Wide Web. |
|
Open-captioned. |
| NLM Unique ID: |
101317945 |
| Other ID Numbers: |
(DNLM)CIT:14042 |
