Peer Exchange Teaser: eCOA and eConsent within Clinical Trials

Pilot trial shows that a user-friendly electronic patient-reported outcome (ePRO) monitoring system significantly improves patient-centered cardiovascular care by enhancing patient-physician communication, increasing clarity in treatment explanations, and empowering patients with better knowledge of their conditions.

Using surveys to collect various viewpoints on eConsent from ethics, sponsors, and vendors.

A use case by Memorial Sloan Kettering Cancer Center explores the potential of EHR-to-EDC.

Five industry leaders share their perspectives on the evolution of DCTs.

Designing eConsent for each study from a stakeholders’ value, not technology perspective.

In part 3 of this video interview with ACT editor Andy Studna, Rohit Nambisan, CEO & founder of Lokavant analyzes some of the most common mistakes he has seen stakeholders make in feasibility studies and how they can be addressed.