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Blockchain protocols in clinical trials: Transparency and traceability of consent

Clinical trial consent for protocols and their revisions should be transparent for patients and traceable for stakeholders. Our goal is to implement a process allowing for collection of patients’ informed consent, which is bound to protocol revisions, storing and tracking the consent in a secure, un...

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Detalles Bibliográficos
Autores principales: Benchoufi, Mehdi, Porcher, Raphael, Ravaud, Philippe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000 Research Limited 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5676196/
https://www.ncbi.nlm.nih.gov/pubmed/29167732
http://dx.doi.org/10.12688/f1000research.10531.5