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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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| Udgivet i: | F1000Res |
|---|---|
| Main Authors: | , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
F1000 Research Limited
2018
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5676196/ https://ncbi.nlm.nih.gov/pubmed/29167732 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12688/f1000research.10531.5 |
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