Clinical investigation capture
Proportionate study data capture
What you get
Capture EDC for proportionate investigations
Structured capture
Longitudinal ePRO and configured site forms in one programme - replace spreadsheets without buying a full Medidata-style EDC.
Automated patient flow
Scheduled follow-up, reminders and missing-data alerts so patients and sites stay on your protocol timeline.
Audit-ready exports
ALCOA+ capture, attested consent, and CSV export for proportionate pre-market and PMCF programmes.
Honest scope
Capture and review software - not a CTMS. Full eCRF query/SDV workflows sit with your CRO or partner EDC where required.
ePRO and site capture
Patient-reported outcomes and clinician baseline forms on one platform - no double entry for the data we own.
Pseudonymised by default
Patient identifiers are separated from study data so your sponsor sees a clean, defensible dataset.
End-to-end study workflow
- Protocol setup - configure PROM schedules, site capture forms, consent, and validation rules with our team.
- Site activation - role-based access, training materials and sandbox environment for each site.
- Patient recruitment - branded patient invites, e-consent and onboarding tracking.
- Data capture - ePRO and configured clinician forms with automated reminders.
- Review and export - clinician review, corrections with reason, CSV and regulated evidence export.
- Analysis handoff - export to your CRO, biostatistician or PMCF evaluation workflow.
Need full eCRF with query management, SDV, and database lock? We integrate as an ePRO and engagement layer or work alongside your existing EDC partner.
Run your next study with us
Tell us about the indication, endpoints and submission target - we'll scope a study build that fits.