WHICH BENEFITS OF RESEARCH PARTICIPATION COUNT AS ‘DIRECT’?
It is widely held that individuals who are unable to provide informed consent should be enrolled in clinical research only when the risks are low, or the research offers them the prospect of direct benefit. There is now a rich literature on when the risks of clinical research are low enough to enrol...
| Authors: | ; ; |
|---|---|
| Format: | Electronic Article |
| Language: | English |
| Check availability: | HBZ Gateway |
| Journals Online & Print: | Drawer...
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| Fernleihe: | Fernleihe für die Fachinformationsdienste |
| Published: |
Wiley-Blackwell
2012
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| In: |
Bioethics
Year: 2012, Volume: 26, Issue: 2, Pages: 60-67 |
| Further subjects: | B
Informed Consent
B vulnerable subjects B fallacy of the package deal B direct benefits |
| Online Access: |
Presumably Free Access Volltext (lizenzpflichtig) Volltext (lizenzpflichtig) |