Wemedoo oomnia ePRO

Increase patient engagement and data quality with oomnia ePRO. Designed as a Bring Your Own Device (BYOD) solution, it allows patients to securely submit data anytime, anywhere, via smartphone, tablet, or web, reducing site burden and improving accuracy. Integrated directly into your study database, ePRO ensures seamless data flow and better trial insights.

Advanced features

Collect patient data in real time using any device, with instant validation and secure syncing.

High data quality

Improve accuracy with automated checks, consistent formats, and ongoing quality monitoring.

Scheduled data collection

Send timely questionnaires and transmit data instantly to EDC and CTMS.

User-friendly design

Boost engagement with a clean interface, multilingual support, and full BYOD compatibility.

Flexible questionnaires

Customize forms with configurable scales and layouts tailored to your trial design.

Benefits

Deploy any ePRO questionnaire with flexible logic, dynamic flows, and full multilingual support.

Full study visibility

Track patient input alongside eCRF data with integrated visual summaries and real-time analytics.

Real-time monitoring

Detect data issues early with synchronized eCRF and ePRO entries for faster intervention.

Error reduction

Avoid transcription mistakes with direct-from-patient entry and instant field-level validation.

Time savings

Speed up setup and delivery with no-code configuration and automated scheduling.

Cost efficiency

Cut costs by using participants’ own devices and reducing manual handling.

Compliant with

• ICH GCP E6

• Good Clinical Data Management Practices, edition 4 (GCDMP)

• Good Automated Manufacturing Practice, edition 5 (GAMP 5)

• FDA 21 CFR Part 820

• FDA 21 CFR Part 11

• Declaration of Helsinki

• ISO 9001:2015 standard

• ISO 27001:2022 standard

• EudraLex, vol. 2 and 4

• GDPR, FADP, and HIPAA