Will Your Labeling Strategy Assure Compliance With EU MDR?

The European medical device industry is a third of the way into a 3-year transitional period that will culminate with full implementation of the EU Medical Device Regulation (EU MDR) in 2020. The new regulation, which entered into force in May 2017, imposes major new rules on companies involved in the design, manufacture, approval and commercialization of devices that are sold in the EU. Will your labeling strategy assure compliance With EU MDR? Download the white paper to find out.