WEBINAR 1 - Tuesday, September 9 | 16:00–17:00 CEST 

Achieving CE marking is just the beginning. This webinar will clarify how Post-Market Surveillance (PMS) and Post-Market Clinical Follow-up (PMCF) requirements shift once your medical device is on the market.

You'll get practical guidance on staying compliant under EU MDR—especially for legacy devices already in use.

What you'll learn:

• Understand how PMS obligations evolve after CE marking
• Learn how to integrate PMCF activities into your PMS strategy
• Discover what notified bodies typically encounter in audits
• Get practical insights on PSURs, PMS reports, and CER updates
• Avoid common pitfalls through real-world examples

WEBINAR 2 - Tuesday, September 23 | 16:00–17:00 CEST

This session dives into the practical side of PMCF. Our team will share how we approach PMCF activities such as clinical investigations, literature reviews, usability studies, and surveys.

A notified body expert will join to provide real audit insights and share what they expect to see in your technical documentation.

What you'll learn:

• Learn how to choose the right PMCF activities for your device
• Understand what notified bodies expect (and flag) in PMCF files
• Hear about common nonconformities and how to avoid them
• Explore workarounds if you lack data or access to patients
• Take away actionable templates and field-tested strategies