Using Research Data Without Your Consent in a Global Health Partnership

Authors

  • 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

DOI:

https://doi.org/10.7202/1058275ar

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.

(c) Emanuelle Dufour

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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.

Issue

Vol. 1 No. 2 (2018): Open Issue

Section

Case studies

License

Copyright (c) 2018 Valéry Ridde

Creative Commons License

This work is licensed under a Creative Commons Attribution 4.0 International License.

The Canadian Journal of Bioethics applies the Creative Commons Attribution 4.0 International License to all its publications. Authors therefore retain copyright of their publication, e.g., they can reuse their publication, link to it on their home page or institutional website, deposit a PDF in a public repository. However, the authors allow anyone to download, reuse, reprint, modify, distribute, and/or copy their publication, so long as the original authors and source are cited.