HOW COVID-19 WILL IMPACT
MEDICAL DEVICE TRENDS
Are you ready for the EU MDR?
The COVID-19 pandemic has created a year-long crisis among healthcare providers and their suppliers. To deal with this crisis, the EU postponed the application date of its MDR regulation. This statute requires medical device makers to produce more information, all translated into the EU’s 24 official languages. This paper explores how COVID-19 will impact medical device trends and outlines the road to full compliance with the new EU MDR regulation.
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