Your private health data vault — with registries built in
Trua lets people and organizations collect, govern, and use health data responsibly. Participants keep control; clinicians and researchers get the tools they need to run ethical, adaptive studies.
What it is
Trua is a participant-centric registry and research platform. It combines a private data vault for individuals with organization-ready tools for consent, identity, survey flows, files, and analytics. Trua respects data residency by deploying jurisdiction-specific nodes, so participant and organizational data stay where they belong.
Core capabilities
Everything you need to run ethical, adaptive registries.
Participant data vaults
Private, encrypted vaults under participant control with clear consent and sharing.
Registry & study tooling
Identity, consent, surveys, file uploads, and cohort views for clinicians and researchers.
Jurisdiction-aware deployment
Residency by design. Regional nodes with independent encryption boundaries and audit trails.
Governance & security
Trua inherits DigitalCabinet’s governance model: ISO-style controls, role-based access, 2-factor authentication, encryption at rest (AES-256) and in transit (TLS), and independent audits — with clear ownership and export pathways.
- Consent and attribution tracked at the record level
- Residency-bound storage with immutable audit logs
- Exit-friendly architecture: export, delete, or migrate on demand
Designed for scrutiny
Trua aligns with GDPR/HIPAA expectations and institutional review requirements. It provides verifiable governance that stands up in audits and ethics reviews.
Trua Loop™ — inside Trua
The Trua Loop is our adaptive ethics pipeline. It turns participant narratives into prioritized outcomes and IRB-ready instruments, enabling continuous, participant-led updates to your studies.
- Open interviews → NLP synthesis → task & outcome statements
- Community prioritization (importance × underservedness)
- Pre-cleared surveys for high-priority unmet needs
Why it matters
Participant voices directly shape study focus. Ethics stays ahead of iteration. Every survey item is traceable back to originating narratives.
Where it’s deployed
Trua powers participant-centric registries and studies across health, rare disease, and public-interest research.
Patient & Participant Registries
Collect longitudinal data responsibly with transparent consent and sharing controls.
Clinician-led Studies
Identity, consent, survey flows, and file capture — all mapped to cohorts and outcomes.
Community & Public Health
Ethical data collaboration with jurisdiction-aware residency and verifiable governance.
Start a registry or migrate to Trua
We’ll scope a discovery sprint and map your governance, residency, and integration needs.
Talk to us