Can we use OpenAI or Claude with patient data?

Yes, with enterprise contract (zero retention, EU region). PII/PHI redaction before the prompt is always recommended. For stricter cases, on-prem Llama/Qwen is the answer.

Is this a medical device?

If it suggests diagnosis — yes, under MDR. We build human-review gates into every high-stakes AI and follow CE-marking workflows when the product ships to market.

AI for Healthcare

Medical AI systems that survive regulatory review

Healthcare AI is unforgiving: accuracy, privacy, auditability. UseAIEasily ships healthtech AI from Budapest for hospitals, clinics, telemedicine, and health SaaS.

Use-cases

Clinical documentation automation: dictated visit → structured note
Report summarization: long medical text → lay and clinical versions
Triage chatbot with disclaimer + human review
Coding assist (ICD-10, CPT)
Drug interaction check with LLM
RAG search over internal protocols
Clinical trial screening: patient recruitment and exclusion

Regulation and safety

EMA/MDR, GDPR, EHR integration, HL7 FHIR. No PHI in public LLMs — enterprise zero-retention API or on-prem only. Every AI decision logged and clinician-reviewed.

EU specifics

EU medical terminology, MDR conformity-aware development, EHR integration, multilingual patient communication.

Build compliance-safe healthtech AI

30-minute call to scope use-case, PHI handling, and regulatory path.

Book a discovery call