Veeva ePRO (electronic Patient Reported Outcomes) captures questionnaire responses directly from clinical trial patients using an app or webpage.
Sponsors manage the ePROs through their own interface, and a central library allows them to reuse ePROs across all their studies.
Sites have a simple access point to manage their participants and can review ePRO data and adherence.
Patients complete the ePRO using MyVeeva for Patients (native application or web), where they can also access other activities like consent or virtual visits. Once complete, the data flows back into the sponsor’s environment.
Where to Start: System Overview for Digital Trials Platform
ePRO Validation Packages: Digital Trials Platform Validation Packages
The following tables outline Veeva’s processes specific to ePRO services:
ePRO Services Processes
For more information on Veeva’s Services, please see Veeva Services