Capturing, validating, and integrating patient data in real time is an important step along the path to cleaner data, timelier decision-making, and accelerated execution in clinical trials. Deployed independently or as part of a full Lunexis™ eSource Ecosystem, our enhanced ePRO+ module streamlines processes through a flexible, unified platform that allows patients and sites a high degree of optionality — and enables sponsors to deploy technology based on the needs of their protocols and patients.
