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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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| Publicat a: | F1000Res |
|---|---|
| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
F1000 Research Limited
2018
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| Matèries: | |
| Accés en línia: | 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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