Post-Market Surveillance in Medical Devices

MS is a legal obligation under EU MDR — but it doesn't have to be a last-minute scramble. Learn how to build surveillance into your development process so the evidence is always ready.

What you'll learn:

• What EU MDR requires from your post-market surveillance programme

• How to embed PMS proactively into the software development lifecycle

• Which device functionalities help gather the evidence notified bodies expect

• How IoT and AI can simplify surveillance and improve evidence quality