If you are a Germany-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!

Together with our partners, we offer you an exclusive free check of your situation with regard to the new regulatory requirements.

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