Our in-house, modular system unifying IRT/IWRS, EDC, CDISC and medical coding on a single database.

What’s included

  • IRT/IWRS — subject & IP management, randomization (dynamic & SAS-based), dashboards
  • EDC — eCRF management, source-data verification, discrepancy & medical coding
  • AI-assisted study & protocol design — adaptive templates, real-time feasibility validation
  • SAP generator & CTA preparation — biostat rules engine, e-signature workflows

Why CEBIS

Most CROs stitch together third-party systems, creating hand-offs where data — and time — leak. We built Trial-HUB® in-house so every module speaks the same language in one secure environment, compliant with 21 CFR Part 11 and ISO 27001 & 9001: real-time visibility for your team and less reconciliation for data management.