EU MDR – Is the Industry Planning for It? Are You?
Whether you’re producing medical devices within Europe or supplying to Europe from the rest of the world, as a manufacturer or supplier, you will need to adhere to the EU MDR by May 2021.
In a survey conducted by PRISYM ID, 26% of respondents admitted that they have just started to think about EU MDR, 24% of respondents admitted that they haven’t started to think about EU MDR and 50% of respondents said they understood the implications and plans are in progress.
Find out what are your peers’ top concerns with regards to EU MDR and what do they think about the areas likely to be affected and about the resources needed to implement the EU MDR.