As the value of patient-reported outcomes is becoming accepted as a critical component by which efficacy outcomes are measured, implementation changes still pose barriers during a clinical trial set up and data collection phases. Traditional methods increase the risk of missing patient safety signals and survey compliance considerations introduce additional complexity into trial design. Streamline the electronic collection of patient-reported data through Medrio’s unified ePRO and EDC platform that can be used anywhere and on any device.
Our Electronic Patient-Reported Outcomes solution handles all of the complexities of patient-reported data, from the flexibility to switch between in-clinic and remote data collection, to the ability to support popular validated survey instruments. Our bring your own device (BYOD) model allows patients to respond to surveys anywhere at any time. Automated notifications ensure compliance with your protocol while boosting patient engagement. The unification of ePRO and EDC allows you to view all of your clinical and patient-reported data in one place and accelerates study build times. Gain faster insights into patient-reported data, more control over timelines, and increased patient engagement.