Published on in Vol 22, No 10 (2020): October

Preprints (earlier versions) of this paper are available at https://preprints.jmir.org/preprint/19129, first published .
Implementation of Electronic Informed Consent in Biomedical Research and Stakeholders’ Perspectives: Systematic Review

Implementation of Electronic Informed Consent in Biomedical Research and Stakeholders’ Perspectives: Systematic Review

Implementation of Electronic Informed Consent in Biomedical Research and Stakeholders’ Perspectives: Systematic Review

Evelien De Sutter 1, MSc;  Drieda Zaçe 2, MD;  Stefania Boccia 2, 3, PhD;  Maria Luisa Di Pietro 2, MD;  David Geerts 4, PhD;  Pascal Borry 5, PhD;  Isabelle Huys 1, PhD

1 Clinical Pharmacology and Pharmacotherapy, Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven , BE

2 Section of Hygiene, University Department of Life Sciences and Public Health, Università Cattolica del Sacro Cuore, Roma , IT

3 Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A Gemelli IRCCS , Roma , IT

4 Meaningful Interactions Lab, KU Leuven , Leuven , BE

5 Centre for Biomedical Ethics and Law, Department of Public Health and Primary Care, KU Leuven, Leuven , BE

Corresponding Author:

  • Evelien De Sutter, MSc
  • Clinical Pharmacology and Pharmacotherapy
  • Department of Pharmaceutical and Pharmacological Sciences
  • KU Leuven
  • O&N II – Herestraat 49 – Box 521
  • Leuven
  • BE
  • Phone: 32 16 37 98 82
  • Email: evelien.desutter@kuleuven.be