Post-Market Surveillance (PMS) has become a fundamental pillar in managing the compliance of medical devices, both within and outside the European Union.

With the introduction of the MDR (EU) 2017/745 and IVDR (EU) 2017/746 regulations, along with specific regulations in non-European markets, companies are required to establish an increasingly robust and proactive post-market system to ensure the safety and effectiveness of their devices throughout their entire lifecycle.

This webinar will explore the updated requirements for PMS systems, analyzing the key differences between Europe and global markets.