Yes. 5thPort supports eConsent across decentralized, hybrid, and traditional in-person clinical trials. Participants can review consent information and complete the consent process remotely (without study staff present) or at the study site, giving sponsors and CROs the flexibility to use the same eConsent platform across different study models and sites.
This also means that the consent experience doesn’t have to change simply because a participant is remote or if a study uses a mix of virtual and in-person interactions.