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Handling eConsent signed by both a Participant and an Investigator for Clinical Trials

In Clinical trials, handling eConsent with two or more parties is important. But what is the most effective way to handle this remotely? Track.Health makes this simple with the smart scheduler.

With the smart scheduler, you can split your PICF into 2 parts, one part for the participant, and one for the investigator. After the participant has completed reading the part This that lets you alert the investigator to sign, after the patient has signed. The patient can do this completely remotely, on their own device.