Medical Device Label: Before And After EU MDR/IVDR

EU MDR introduces additional information that needs to be included on labels, forcing organizations to design new label templates that make room for data not previously part of the labeling system. It’s both a design and a data challenge, and they must quickly be addressed to avoid a sticky situation. This article presents 10 points to keep in mind when working with EU MDR/IVDR regulations. Download the full paper for more information.