Minimal or reasonable? Considering the ethical threshold for research risks to nonconsenting bystanders and implications for nonconsenting participants.

When research poses risks to non‐participant bystanders, it is not always practicable to obtain their consent. One approach to assessing how much research risk may be imposed on nonconsenting bystanders is to examine analogous circumstances, including risk thresholds deemed acceptable for nonconsent...

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Publicado en:	Bioethics Vol. 34; no. 9; pp. 923 - 933
Autor principal:	Fernandez Lynch, Holly
Formato:	Artículo
Publicado:	Wiley-Blackwell Nov2020
Materias:	United States Bioethics Informed consent (Medical law) Research ethics Human research subjects Risk assessment Risk management in business Patient selection
Acceso en línea:	Ver este registro en EBSCOhost