Unified clinical-trial data pipeline for governed trial readout.

Problem

Phase III readouts can slip when data from CROs, EHRs, and lab vendors is reconciled by hand. Each new trial can add recurring data-engineering toil and an audit trail stakeholders do not trust.

Solution

A representative build uses a vendor-agnostic pipeline that ingests CDISC, FHIR, and proprietary CRO formats into a governed lakehouse with full lineage. Trial-specific dbt models, eval harnesses, and privacy-aware observability ship as part of every new trial setup, not after.

Outcome

The representative target is faster trial setup, cleaner lineage, and a data-integrity audit path that can be reviewed without rebuilding evidence by hand.