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Clinical Trial Automation

Purpose-Built for Regulated Trial Data

Trialhelix is designed for CROs running Phase I and II programs. From first eCRF to final CDISC dataset — one connected workflow with a 21 CFR Part 11 aligned audit trail.

Study Build in Days, Not Weeks

Typical Phase I protocol delivered in 4–6 days. EDC configuration, visit schedule, and edit checks in one workflow.

CDISC Delivery Without SAS Overhead

22+ SDTM domains auto-mapped from eCRF. No dedicated SAS programmer required for initial dataset package.

~60% Query Cycle Time Reduction

Automated query generation and resolution tracking vs manual query generation workflows.