Personalized and long-term electronic informed consent in clinical research: stakeholder views

BACKGROUND: The landscape of clinical research has evolved over the past decade. With technological advances, the practice of using electronic informed consent (eIC) has emerged. However, a number of challenges hinder the successful and widespread deployment of eIC in clinical research. Therefore, w...

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Detalles Bibliográficos
Autores principales: De Sutter, Evelien, Borry, Pascal, Geerts, David, Huys, Isabelle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8325412/
https://www.ncbi.nlm.nih.gov/pubmed/34332572
http://dx.doi.org/10.1186/s12910-021-00675-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8325412/
https://www.ncbi.nlm.nih.gov/pubmed/34332572
http://dx.doi.org/10.1186/s12910-021-00675-7

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