Electronic Clinical Outcome Assesment (eCOA)
Set-up your CE marked EDC fast, collect high quality clinical data (eCOA) and monitor the process in a single or multi-center trial. Your Research offers the most innovative modules (eCRF, ClinRO, ePRO, PerfO, ObsRo) to collect data, role based access and the possibility to notify on key decisions and monitoring.
Fast and efficient implementation of study design
- Use a form builder that is designed for non-IT people.
- Complex score calculations and field validations.
- Re-use pre-defined data fields or (validated) forms from the library.
Access management and monitoring
- Intuitive dashboard for key decision support inclusion criteria, adverse events and process ad-herence.
- Configure permissions on study, role and individual level.
- Real time data validation support.
Data management, import and export
- Export data via CSV, SPSS or API or via pre-defined reports.
- Connect devices, electronic health records or other sources through our API, HL7 or FHIR.
- CFR Part 11 compliant audit trail.
Other modules
Connect other modules to collect data, engage your patient and streamline your study.
Module ePRO
- Subjects reporting via smartphone or computer
- Questionnaires, diaries or connect devices
- Researcher dashboard for monitoring and key decisions
Module ObsRo
- Involve family member or caregivers
- Health related outcomes of the subject reported
Module eCRF
- Set-up your forms easily
- Capture data form different sources
Module eConsent
- Inform subjects interactive
- Streamline your eConsent proces
- Less administrative burden
Module eVisit
- Inform subjects about their coming visit
- Self scheduling through subjects on time slots
- Videocalling with subjects
