EU MDR/IVDR: Updated List of National Contact Points Released

The European Commission has recently published an updated document listing the National Contact Points for the Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR).

This document serves as a vital resource for manufacturers, distributors, and stakeholders in the medical device industry, providing direct access to the competent authorities across EU member states.

Highlight of the Latest Update:

Estonia: The contact details for the State Agency of Medicines have been revised.

Staying up-to-date with regulatory changes is essential for ensuring compliance and facilitating smooth communication with national authorities.

You can download the full document with all updated contact points by clicking the link below