Synchronize the path to regulatory approval
Comprehensive governance and data exchange that unlocks patient journeys before, during and after clinical trials
With high error rates from legacy technologies, we believe the token is broken, limiting life sciences organizations from realizing the full potential of real-world data (RWD) in maximizing the investment in clinical trials. HealthVerity FLOW for Clinical Trials is the only pharma-grade solution that can synchronize patients across de-identified, identifiable and investigator data, all in a fully governed, HIPAA-compliant and 21 CFR 11-certified environment. Powered by the IPGE approach, this end-to-end SaaS solution optimizes trial insights throughout the clinical research stages, from recruitment and enrollment screening to external control arm and long-term followup studies.
The ultimate source of truth
To ensure the most accurate and data-driven outcomes, begin your clinical trial journey with HealthVerity Identity Manager, the industry’s most accurate solution for patient matching and identity resolution. Serving as the single source of truth for enrolled patients across the enterprise, HealthVerity offers a reliable platform to track and manage patient participation over time, while preserving the option to seamlessly retrieve patient-centric de-identified or identifiable
Built-in privacy and consent management
Confidently manage both identifiable and de-identified data, patient consents and user permissions throughout the study and beyond. This 21 CFR Part 11-certified solution fully integrates with eConsent systems in addition to offering a distributed webform for site-level data capture.
On-demand data discovery
Unlock patient journeys before, during and after clinical trials with on-demand real-world data discovery and delivery from the nation’s largest healthcare and consumer data ecosystem. Overlap your trial cohorts in real-time across the universe of RWD in HealthVerity Marketplace to explore comorbidities, biomarkers or important physician notes, all in a HIPAA-compliant manner. Just as easily retrieve a wide breadth of identifiable patient data for those who have given consent to further generate real-world evidence in combination with your investigator findings.
From pre-trial to approval and beyond: Enhance your clinical trial research with real-world data
More and more pharma companies are incorporating RWD into their new drug applications because it works. This white paper discusses the benefits, challenges and solutions to this innovative approach.