To establish compliance with the Medical Device Regulation (EU) 2017/745, manufacturers need to establish conformity to all the relevant GSPRs. Do you know how to determine the relevant GSPR requirements? How different are the GSPRs from the ERs? What data is required for demonstrating conformity with different GSPRs? Decode comprehensive insights as Smridula Hariharan from Freyr discusses in her thought leadership published in MPO magazine.