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BMC Health Services Research|February 22, 2023
Informing a European guidance framework on electronic informed consent in clinical research: a qualitative studyEvelien De Sutter, Pascal Borry, Isabelle Huys, et al.BMC Medical Ethics|August 1, 2021
Personalized and long-term electronic informed consent in clinical research: stakeholder viewsEvelien De Sutter, Pascal Borry, David Geerts, et al.Frontiers in Medicine|June 13, 2022
Digitizing the Informed Consent Process: A Review of the Regulatory Landscape in the European UnionEvelien De Sutter, Janos Meszaros, Pascal Borry, et al.Talanta|July 26, 2017
Analysis of illegal peptide drugs via HILIC-DAD-MSSteven Janvier, Evelien De Sutter, Evelien Wynendaele, et al.Frontiers in Pediatrics|September 20, 2021
Clinical Research in Neonates: Redesigning the Informed Consent Process in the Digital EraEvelien De Sutter, Birte Coopmans, Femke Vanendert, et al.Journal of Medical Internet Research|December 19, 2023
Testing and Practical Implementation of a User-Friendly Personalized and Long-Term Electronic Informed Consent Prototype in Clinical Research: Mixed Methods StudyEvelien De Sutter, David Geerts, Koen Yskout, et al.Digital Health|January 25, 2024
Personalized and longitudinal electronic informed consent in clinical trials: How to move the needle?Evelien De Sutter, Liese Barbier, Pascal Borry, et al.Journal of Medical Internet Research|October 8, 2020
Implementation of Electronic Informed Consent in Biomedical Research and Stakeholders' Perspectives: Systematic ReviewEvelien De Sutter, Drieda Zaçe, Stefania Boccia, et al.Digital Health|July 5, 2022
Co-creation with research participants to inform the design of electronic informed consentEvelien De Sutter, David Geerts, Pascal Borry, et al.Frontiers in Medicine|October 14, 2022
Rethinking informed consent in the time of COVID-19: An exploratory surveyEvelien De Sutter, Teodora Lalova-Spinks, Pascal Borry, et al.Pageof 2