ePRO is a patient-centric Electronic Patient-Reported Outcomes solution designed to capture high-quality patient-reported data in real time during late-phase clinical trials. By enabling secure, flexible data collection through intuitive digital tools, ePRO improves patient engagement, data completeness, and regulatory compliance while supporting both on-site and remote participation.
Improves patient participation through intuitive, patient-friendly digital tools that keep patients engaged throughout the study.
Ensures accurate and complete patient-reported data capture while reducing missing or delayed entries.
Supports higher adherence and retention rates through structured interactions and timely reminders.
Reduces site workload related to patient follow-ups and data collection activities.
Provides rapid access to patient-reported outcomes for timely analysis and informed decision-making.
Ensures secure, traceable, and audit-ready patient data aligned with regulatory requirements.
