Frequently Asked Questions About Medical Devices

 

The EU’s Medical Device Regulation (MDR) was officially published on 5 May 2017 and came into force on 25 May 2017. The MDR will replace the EU’s current Medical Device Directive (93/42/EEC) and the EU’s Directive on active implantable medical devices (90/385/EEC).

 

In this whitepaper, you can benefit from the frequently asked questions regarding MDR and EUDAMED.

 

 

Insights

More Related Articles

Sustainability Report 2025

Italy Medicines Traceability Compliance: Preparing for the NMVO Italia Enforcement Phase

SoftGroup Receives EcoVadis Committed Badge