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...

Descripción completa

Detalles Bibliográficos
Publicado en:Bioethics Vol. 26; no. 2; pp. 60 - 68
Autores principales: Friedman, Alexander, Robbins, Emily, Wendler, David
Formato: Journal Article
Publicado: Wiley-Blackwell Feb2012
Acceso en línea:Ver este registro en EBSCOhost