This paper is in the following e-collection/theme issue:

Focus Groups and Qualitative Research for Human Factors Research (852) Ethics, Privacy, and Legal Issues (479) Electronic/Mobile Data Capture, Internet-based Survey & Research Methodology (832) Secondary Use of Clinical Data for Research and Surveillance (367) Big Data (240) Policy (56) Health Information Exchange (98)

Published on in Vol 9, No 3 (2022): Jul-Sep

Preprints (earlier versions) of this paper are available at https://preprints.jmir.org/preprint/36797, first published .
Patients’ and Publics’ Preferences for Data-Intensive Health Research Governance: Survey Study

Patients’ and Publics’ Preferences for Data-Intensive Health Research Governance: Survey Study

Patients’ and Publics’ Preferences for Data-Intensive Health Research Governance: Survey Study

Authors of this article:

Sam H A Muller1 Author Orcid Image ;   Ghislaine J M W van Thiel1 Author Orcid Image ;   Marilena Vrana2 Author Orcid Image ;   Menno Mostert1 Author Orcid Image ;   Johannes J M van Delden1 Author Orcid Image
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