Contivra for Healthcare
Governed data for clinical AI and research. PHI-safe, HIPAA-compliant, research-grade data governance that accelerates clinical innovation without compromising patient privacy.
Privacy-Safe Data Governance at Scale
Healthcare organisations hold the most sensitive data in the enterprise. Contivra provides the governance infrastructure to unlock that data for AI and research—safely, compliantly and with full audit trails that satisfy regulators and ethics boards.
- PHI detection, classification and de-identification governance at column level
- Clinical trial data lineage and full audit trails for regulatory submissions
- Real-world evidence data products with quality SLAs and source provenance
- Cross-institution data sharing with patient-level access policy enforcement
- HIPAA and GDPR compliance with immutable audit trails for every data access
- AI model governance with feature lineage for clinical decision support systems
Where Contivra Delivers Value
Clinical AI Governance
Govern the training data, features and outputs of clinical AI models—with full lineage, quality scores and explainability required by FDA and EMA.
Pharmacovigilance Data
Unified adverse event data with source lineage and quality monitoring—meeting post-market surveillance obligations with auditable, traceable data.
Real-World Evidence
Certified real-world evidence data products built from EHR, claims and registry data—with privacy-preserving governance and quality SLAs.
Regulatory Submissions
End-to-end data lineage from source systems to submission-ready datasets—accelerating NDA, BLA and HTA submissions with complete data provenance.
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