Blockchain protocols in clinical trials: Transparency and traceability of consent [version 3; referees: 1 approved, 2 approved with reservations, 1 not approved]

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 the collection of patients’ informed consent, which is bound to protocol revisions, storing and tracking the consent in a secure, un...

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Bibliographic Details
Main Authors: Mehdi Benchoufi, Raphael Porcher, Philippe Ravaud
Format: Article
Language:English
Published: F1000 Research Ltd 2017-07-01
Series:F1000Research
Subjects:
Online Access:https://f1000research.com/articles/6-66/v3