Patients in prospective and real-world studies still report on paper, or have to attend a visit for information that could be captured at home.
Investigators leave data points out because collecting them means extra visits or extra cost, and complex protocols drive early drop-out and low inclusion.
An ePRO app and web route, configured to the protocol, with a site and study dashboard covering protocol adherence and compliance, digital consent collection, and integration into the electronic case report form and patient record workflows.
The CRO's real-world evidence team assembles the modular building blocks per sponsor request. We provide the technical setup, maintenance, updates and the evidence integration.
Tell us what you are working on and we will help you get it moving.
