REGULATORY AFFAIRS

Post Market Surveillance under the EU MDR – Challenges and Best Practices

29th Jan, 2025 3:00 PM - 4:30 PM GMT - Michelle Keane

Post Market Surveillance under the EU MDR – Challenges and Best Practices

This is a Free Comply Guru Webinar where Post-Market Surveillance under the EU MDR – Challenges and Best Practices will be discussed by Michelle Keane.

eu mdr medical devices medtech post market surveillance regulatory affairs

Technical Documentation under the EU MDR 2017/745

12th Dec, 2024 4:00 PM - 5:00 PM GMT - Orla Keane

Technical Documentation under the EU MDR 2017/745

This is a Free Comply Guru Webinar where Technical Documentation under the EU MDR will be discussed by Michelle Keane and Orla Keane.

eu mdr medical devices regulatory affairs technical documentation