EU data residency (design)
Patient and visit data are designed for processing and storage in European regions under contractual enterprise controls.
Trust & security
Privacy-first clinical intelligence for Europe.
VitaTwin is built for consent, clinician control, and European data expectations, without overstating certifications. Honest roadmap language; real safety in the product demos.
Consent-controlled twin
Every partner connection is scoped by the patient. Clinicians see only what was granted for that encounter.
No long-term audio retention (roadmap)
Ambient capture demos discard audio after transcription in the target architecture. Notes are not keyed as raw patient audio archives.
Human oversight
Notes, codes, and CDS answers require clinician review. VitaTwin does not auto-commit to the chart.
Non-diagnostic by default
Outputs are decision-support only. Crisis safety flags escalate; harmful guidance is refused.
Built toward European regulation
Product and QMS workstreams align with GDPR and medical-device readiness (ISO / MDR path). We do not claim CE marks we do not hold.
What we will never claim falsely
Until independently certified, VitaTwin will not display MDR Class IIa CE marks or ISO badges as product facts. We describe intent, safeguards already in demos, and the path to regulated clinical AI in the EU and DACH markets.