Join us for an exclusive free check of your situation with regard to the new regulatory requirements.

If you are an Italian-based company with questions induced by the new MDR (classification, clinical testing & quality management of medical devices, and in vitro diagnostics), this event is for you!

During 1 hour, our Medidee experts will answer your questions and will guide you to the next steps!

Find out more and sign up for free 👉 here

⚠️ Hurry, slots go fast! First come, first served ⚠️

Medidee – Compliance with Relevance