EU MDR Labeling Compliance: Learning The Lessons From UDI
The European medical device industry is in the grip of the biggest changes the market has seen in decades.
EU MDR (European Medical Device Regulations) ensures the safety of medical devices sold in the EU. Anybody involved in the design, manufacture, approval and commercialization of devices is affected and will need to updated their processes.
Read our whitepaper “EU MDR Labeling Compliance: Learning the Lessons from UDI " to find out the significant ramifications the regulation have on labeling operations.