Veeva Systems announced the availability of Veeva ePRO, a key advancement in patient-centric digital trials. The application makes it easier for patients to complete assessments on a mobile device or web browser and enables real-time data access for sponsors and clinical research sites. As part of a connected platform for clinical trials, study teams can use ePRO to exchange high-quality data across the clinical ecosystem for improved transparency and collaboration.
According to research sites, the top challenges in patient retention include the time required to participate in a trial, repetitive information requests, and time spent entering data.1 Veeva ePRO improves the patient experience by providing a modern, user-friendly application for completing Patient-Reported Outcomes (PRO).
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The application also helps streamline trial activities for sponsors and research sites. Sponsors can configure studies using survey and instrument libraries and push ePRO and schedule definitions to research sites. Research sites can then easily assign activities, automatically receive updates, and track patient progress without needing other systems or applications.
“Veeva ePRO is built to meet the needs of patients, sites, and sponsors, and is connected for end-to-end execution,” said Tim Davis, vice president of strategy, MyVeeva for Patients at Veeva. “We are committed to partnering with customers to deliver modern digital applications that help the life sciences industry advance to patient-centric digital trials.”
Veeva ePRO is part of Veeva Vault Clinical Suite, the industry’s first cloud platform that unifies clinical data management and operations.