Cargando…
Digitizing the Informed Consent Process: A Review of the Regulatory Landscape in the European Union
BACKGROUND: Rapid technological advancements are reshaping the conduct of clinical research. Electronic informed consent (eIC) is one of these novel advancements, allowing to interactively convey research-related information to participants and obtain their consent. The COVID-19 pandemic highlighted...
Autores principales: | De Sutter, Evelien, Meszaros, Janos, Borry, Pascal, Huys, Isabelle |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9174519/ https://www.ncbi.nlm.nih.gov/pubmed/35692551 http://dx.doi.org/10.3389/fmed.2022.906448 |
Ejemplares similares
-
Informing a European guidance framework on electronic informed consent in clinical research: a qualitative study
por: De Sutter, Evelien, et al.
Publicado: (2023) -
Clinical Research in Neonates: Redesigning the Informed Consent Process in the Digital Era
por: De Sutter, Evelien, et al.
Publicado: (2021) -
Personalized and long-term electronic informed consent in clinical research: stakeholder views
por: De Sutter, Evelien, et al.
Publicado: (2021) -
Rethinking informed consent in the time of COVID-19: An exploratory survey
por: De Sutter, Evelien, et al.
Publicado: (2022) -
Implementation of Electronic Informed Consent in Biomedical Research and Stakeholders’ Perspectives: Systematic Review
por: De Sutter, Evelien, et al.
Publicado: (2020)