The Ethics of Informed Consent for Data Registries: Moving Beyond Moral Minimalism to the High Ground.

There is a rapid increase in disease registries all over the world, propelled by innovations in electronic health records and computer technologies. Unlike the developed world, where many registries are well established, many disease registries in the developing world are still in their incipient st...

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Publicado en:	Bioethics Vol. 39; no. 7; pp. 709 - 716
Autor principal:	Chingarande, George Rugare
Formato:	Artículo
Publicado:	Wiley-Blackwell Sep2025
Materias:	Policy sciences Responsibility Information technology Informed consent (Medical law) Medical research Data transmission systems Data management Professional practice Reporting of diseases Electronic health records
Acceso en línea:	Ver este registro en EBSCOhost