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FAQ

Frequently Asked Questions

Welcome to the Med-CertifAI MDR Assistant!

Our AI-powered assistant is trained specifically on the European Medical Device Regulation (EU MDR 2017/745). Whether you’re looking for clarification on classification rules, technical documentation requirements, or post-market surveillance, the MDR Assistant is here to help.

✅ Ask any question related to MDR certification.
✅ Get professional, clear, and concise answers instantly.
✅ Save time and reduce uncertainty during your compliance journey.

The MDR Assistant provides general guidance based on the EU MDR. For project-specific advice, we recommend consulting a qualified regulatory affairs expert.