Streamline Patient-Reported Outcomes for More Reliable Clinical Data
Clinion ePRO empowers clinical trials with real-time, secure data capture, boosting patient engagement and retention. With multilingual support and a user-friendly interface, patients can easily report outcomes from their own devices, reducing dropout rates and improving data quality. Clinion ePRO’s seamless integration ensures you have the insights you need, faster.
Our tool generates up to 90% of the draft within minutes with just your protocol synopsis as input, cutting weeks of manual effort.
The tool uses the ICH M11 template ensuring generated protocols meet ICH guidelines and adhere to industry standards.
Clinion ePRO seamlessly scales across trials of all sizes, from small studies to large-scale trials with 20,000+ patients, ensuring efficient data management across sites and regions.
Patients Report Data
Submit responses via mobile or web with automated reminders.
Validation & Syncing
Real-time integration with Clinion EDC/ standalone ensures data accuracy and compliance.
Site & Sponsor Review
Trial teams access real-time patient-reported outcomes for immediate insights.
Actionable Decisions & Reporting
High-quality data enables faster decision-making and regulatory submission readiness.
Transform Patient-Reported Data into Actionable Insights
Seamless & Intuitive Data Capture
A user-friendly UX with multilingual support allows effortless data entry across mobile, tablet, and web. Push notifications and automated reminders ensure timely submissions.
BYOD Model & Offline Accessibility
Patients can use their own devices for data entry, even in offline mode. Data syncs automatically when reconnected, ensuring authentic and unmanipulated information.
Customizable & Efficient Forms
Pre-built templates and dynamic forms are designed to adapt to specific trial needs. This reduces setup time while maintaining high levels of accuracy and consistency.
Real-time Monitoring & Integration
Seamless integration with Clinion EDC or standalone systems enables real-time oversight. This ensures data integrity and completeness for more efficient trials.