Informed consent used to take place on lengthy, hard to comprehend paper consent forms, during in-person for patients who were within travel distance to a physical site. Today, we have an easier, more accessible solution called eConsent. eConsent not only enables remote consenting, accelerating the patient screening and enrollment process, but also enhances patient comprehension resulting in increased retention, trial efficiencies and cost savings. It’s why 59% of clinical trial investigators expect eConsent adoption to increase post-Covid-19.
Is there any reason why you wouldn’t upgrade?
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