FAQs

Frequenty Asked Questions

We collaborate with hospitals, pharma, MedTech, and research institutions worldwide.

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Comprehensive guidance on our platform, security, compliance, and clinical impact

Privacy & Compliance

Hospitals remain the data controllers. Savana acts as a processor under strict Data Processing Agreements.

Within the operational region: EU (AWS EU), UK, or US regional clouds. Always encrypted, segregated, and compliant.

By design, no. Any exception requires a clear legal basis and safeguards (GDPR, EHDS, HIPAA).

When data are fully anonymized, consent is not required by regulation. Local ethics boards may request additional approval.

All identifiers are pseudonymized, free text is de-identified, no PII is displayed, and every access is audited.

Security & Technology

Role-based access control, MFA, least-privilege policies, and immutable audit logs.

It is trained exclusively on real-world EHRs, multi-language by design, and clinically validated – unlike generic NLP engines.

LLMs are general-purpose and probabilistic. Savana’s cNLP is deterministic, explainable, and validated for regulated healthcare use.

Going beyond structured fields to extract insights from the full richness of clinical notes, enabling higher-resolution RWE.

Scientific Guarantees & Differentiation

Independent clinical annotation, precision/recall benchmarks ≥95%, peer-reviewed publications, and bias-mitigation frameworks.

ISO 27001/27701, compliance with GDPR/EHDS/HIPAA, interoperability with OMOP/FHIR, and regular third-party audits.

By combining multilingual clinical NLP, privacy-by-design, full auditability, and proven scientific output across hundreds of real-world studies.

Governance & Transparency

Third parties regularly audit security, privacy, and scientific methodology, in addition to internal compliance checks.

A formal incident response plan ensures rapid detection, notification, and remediation, always within regulatory timelines.

Methods are peer-reviewed, results are published, and regulatory bodies are engaged early when projects inform clinical practice or approvals.

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