Built a HIPAA-compliant web platform unifying data from 200+ clinical trial sites, replacing fragmented spreadsheets with a single source of truth for research teams across 12 countries.
The client managed clinical trials across 200+ sites globally. Each site submitted data in different formats—Excel, CSV, custom EDC systems—requiring weeks of manual reconciliation before analysis. Data quality issues went undetected for months. Regulatory inspectors required demonstrable data lineage that their fragmented workflow could not provide.
We developed a React-based web application with a Go backend supporting standardized data ingestion pipelines, automated quality validation, and a role-based dashboard for research coordinators, principal investigators, and regulatory teams. The platform enforces CDISC data standards at ingestion and provides real-time study progress visualization.
3 weeks to 4 hours
Data reconciliation time
200+ across 12 countries
Active trial sites
Automated within 15 minutes
Data quality issues detected
Achieved in first audit
Regulatory audit readiness