¾ÅÉ«ÊÓƵ

The ¾ÅÉ«ÊÓƵ 2022 European Medical Device Industry Report provides insight into the latest regulation modifications to Regulation (EU) 2017/745 (MDR). It examines how, although not as mature as the pharmaceutical regulatory ecosystem, the European medical device regulatory landscape is beginning to follow a similar path, and how linguistic requirements are an integral part of this complex ecosystem. 

This report covers: 

• Regulations and processes comparison between MDR and Pharma 
• Key linguistic factors that affect market prospects 
• Structural blindspots between the two regulations 
• Centralised solutions to address these new requirements and facilitate medical device manufacturers ability to continue business as usual