Trial Data OS


Easy to use:

No geographical restrictions, subjects can give informed consent at home Transparent and traceable informed process Real-time communication between investigator and subject with fully informed process to effectively protect the rights of subjects

Convenient for everyone:

Support both on-site and remote clinical studies Ensure the use of correct version in each site Quickly notify and sign the updated version of ICF
Trial Consent is a subject-centric eConsent tool. Use plain language and multimedia interaction (photos, videos, etc.) throughout the study, which allows the subjects to quickly and fully understand the study, making the subjects feel more involved. At the same time, it can also ensure that the subjects are fully informed by the investigators.