EU MDR Labeling Compliance: Learn The Lessons From UDI

As part of the MedTech Summit Digital Week we are sponsoring and presenting a webinar on EU MDR, featuring two industry experts, Mark Cusworth and Andrew Love.

EU MDR is being viewed as an extension of the FDA’s UDI (Unique Device Identification), but also a ‘step up’. However, it’s more detailed and more complex due to the local language requirements needed for Europe.

The introduction of UDI requirements into the EU is good news for organizations that are already along the pathway of adopting systems and processes to support FDA UDI compliance. However, for those that aren’t – and indeed those that may have made only basic adjustments to their labeling infrastructure in response to the regulations – there are five key learnings that have emerged from the UDI experience that may help inform best practice adoption with EU MDR.

Join us for this 60-minute information packed webinar to discover why EU MDR will change the medical device labeling landscape globally and how to best meet the impending challenges.