ePRO
Our ePRO module enables patients and clinicians to report outcomes electronically using web-based platforms or handheld devices. By eliminating paper diaries and manual data entry, ePRO ensures that clinical trial outcomes are captured accurately in real time.
With secure digital access, participants can directly record their experiences, symptoms, and quality-of-life measures. Physicians and trial teams gain instant access to validated patient data, improving study accuracy and compliance.
Product Features
Our ePRO solution is built to simplify how patients and clinicians report outcomes while ensuring compliance and data integrity.
Implementing ePRO enhances patient engagement and delivers higher quality clinical outcomes data.
Digitize your outcomes reporting process with our ePRO solution.
Digitize your outcomes reporting process with our ePRO solution.
📅 Book a Demo or 📥 Download our ePRO Brochure to discover how patient-centric technology improves trial outcomes.
Can patients without smartphones use ePRO?
Yes, patients can report outcomes through web portals or provided devices.
Is ePRO data legally valid?
Yes, it complies with 21 CFR Part 11 and global regulatory requirements.
Can questionnaires be customized for different studies?
Absolutely, our system supports fully customizable forms and templates.
How do you reduce missing data?
Automated reminders and notifications ensure patients complete entries on time.
Can ePRO integrate with EDC and CTMS systems?
Yes, seamless integrations keep all your clinical data connected and consistent.