
HealthVerity’s Clinical Trial Linkage synchronizes patient journeys with real-world data before, during and after trials, enabling secure, HIPAA-compliant insights, long-term follow-up, and optimized trial outcomes through advanced identity resolution and data governance.
Vendor
HealthVerity
Company Website

HealthVerity for Clinical Trial Linkage
HealthVerity for Clinical Trial Linkage is a comprehensive, unified solution designed to synchronize clinical trial participants with their real-world data (RWD) across all phases of research. It enables life sciences organizations to unlock complete patient journeys before, during, and after clinical trials in a fully governed, HIPAA-compliant, and 21 CFR Part 11-certified environment. Powered by HealthVerity Identity Manager, this platform enhances trial insights, supports regulatory readiness, and ensures accurate patient matching and data linkage.
Features
- End-to-end synchronization of patient journeys across clinical trials and RWD
- Powered by HealthVerity Identity Manager for precise identity resolution
- HIPAA-compliant and 21 CFR Part 11-certified infrastructure
- Real-time cohort overlap with HealthVerity Marketplace data
- Built-in privacy and consent management tools
- On-demand data discovery and delivery from the largest healthcare and consumer data ecosystem
- Support for retrospective histories, long-term follow-up, and post-trial surveillance
- Enterprise-wide visibility across Phase II, III, and IV trials
Capabilities
- Link trial participants to de-identified or identifiable RWD with full data provenance
- Retrieve patient data on-demand, often within the same day
- Track and manage patient participation over time
- Enable contextualization of patient data for FDA RWD guidance
- Capture data from outside trial sites to enrich trial datasets
- Explore comorbidities, biomarkers, and physician notes in real-time
- Store, manage, and report patient participation securely
Benefits
- Accelerates regulatory approval through verified data linkage
- Reduces error rates compared to legacy token-based technologies
- Improves trial efficiency and data accuracy
- Enhances visibility into patient journeys beyond trial boundaries
- Supports compliance with privacy and consent regulations
- Facilitates better decision-making with enriched RWD insights