Using Research Data Without Your Consent in a Global Health Partnership

  • Valéry Ridde Centre Population et Développement (CEPED), Institut de Recherche pour le Développement (IRD), Université Paris Descartes, INSERM, équipe SAGESUD, Paris, France; Institut de recherche en santé publique de l'Université de Montréal (IRSPUM), Montréal, Québec, Canada; Département de médecine sociale et préventive, École de santé publique de l'Université de Montréal (ESPUM), Montréal, Canada
Keywords: partnership, global health, data, ethics, trust
Language(s): French

Abstract

Global health research is most often spent in a context of international collaboration, particularly North-South. The particular context of this type of partnership (power, money, distance, norms, training, etc.) can lead to important issues in the use of the data collected. This case study enables the reader to reflect on this particular issue and the actions that could be taken to deal with it.

Published
2018-02-27
How to Cite
[1]
Ridde V. Using Research Data Without Your Consent in a Global Health Partnership. Can. J. Bioeth. 2018;1:22-3. https://doi.org/10.7202/1058275ar.
Section
Case studies