The obvious appeal and growing momentum of clinical ethics in academic medical centers should not blind us to a potential danger: the collapse of critical distance. The very integration into the clinical milieu and the processes of clinical decision making, that clinical ethics claims as its greates
Reflections of an ethicist: Research ethics committees and the investigator?a healthy partnership?
โ Scribed by Farnell, S.M.
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 41 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0098-1532
No coin nor oath required. For personal study only.
โฆ Synopsis
Any institution in the USA that receives federal funding must submit research protocols to an IRB. An IRB must conform to federal regulations ''if the federal government has funded the research. . . . Currently, federal regulation does not require IRB review of privately funded protocols, unless they are subject to FDA regulations'' (4). 2 Guidelines for the organisation and responsibilities of IRB and LREC are similar. See: Department of Health (DoH).
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