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Medical AI compliance, built into your workflow

Epok classifies your model under the EU AI Act, generates your technical documentation, and gets you to audit-ready — in minutes, not months.

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Instant classification

Describe your model's intended use and get your EU AI Act risk classification in seconds — deterministic, auditable, and traceable to specific articles.

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Documentation starter pack

8 pre-filled regulatory documents — from intended purpose to declaration of conformity — generated from your inputs and ready for expert review.

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Built for medical AI

EEG-specific hazard libraries, PCCP flagging for continuous-learning systems, and growing MDR support — purpose-built for the healthcare domain.

From intended use to conformity declaration

Answer a few questions about your medical AI model and Epok generates 8 pre-filled regulatory documents, each traceable to specific EU AI Act articles. Review, complete, and export — in PDF or DOCX.

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descriptionRisk Management PlanDraft
check_circleSystem identification
check_circleHazard analysis
check_circleRisk evaluation
check_circleRisk control measures
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