WHICH BENEFITS OF RESEARCH PARTICIPATION COUNT AS 'DIRECT'?
ABSTRACT 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...
| Publicado en: | Bioethics Vol. 26; no. 2; pp. 60 - 68 |
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| Autores principales: | , , |
| Formato: | Journal Article |
| Publicado: |
Wiley-Blackwell
Feb2012
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| Acceso en línea: | Ver este registro en EBSCOhost |