EU Medical Device Regulation for combination products

Do you work with at the crossroads of medtech and pharma developing combination products? Are you a pharma professional that needs to learn more about EU Medical Device Regulation (MDR)? 

Join Läkemedelsakademin for this intro course to EU Medical Device Regulation for combination products on October 25th in Stockholm to gain a better understanding of medical devices and the requirements introduced by the new European regulation MDR. 

Register now

Medical equipment in the ICU ward