10 Steps To EU MDR Labeling Implementation

The European medical device industry is in the grip of the biggest change the market has seen in decades and the European Medical Device Regulation (MDR) and In Vitro Diagnostic Device Regulation (IVDR) ensures high standards of quality and safety for medical devices being produced in or supplied into Europe. Whether producing medical devices within Europe or supplying to Europe from the rest of the world, a manufacturer or supplier will need to adhere to the new EU MDR. This white paper presents 10 steps required to make the implementation of EU MDR labeling simpler. Download the full paper for more information.