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, Belgium
2
Section of Hygiene, University Department of Life Sciences and Public Health, Università Cattolica del Sacro Cuore, Roma, Italy
3
Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A Gemelli IRCCS, Roma, Italy
4
Meaningful Interactions Lab, KU Leuven, Leuven, Belgium
5
Centre for Biomedical Ethics and Law, Department of Public Health and Primary Care, KU Leuven, Leuven, Belgium
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, 3000
-
Belgium
-
Phone:
32 16 37 98 82
-
Email: evelien.desutter@kuleuven.be