eu mdr | Comply Guru Finland

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

29th Jan, 2025 5:00 PM - 5:45 PM ETT - 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

Four Considerations when Internal Auditing under the EU MDR Webinar

10th Jul, 2024 5:00 PM - 6:00 PM BST - Michelle Keane

Four Considerations when Internal Auditing under the EU MDR Webinar

This is a Free Comply Guru Webinar on Key Considerations when Internal Auditing under the EU MDR with Michelle Keane.

eu mdr internal auditing medical devices

CQI & IRCA Approved Training Provider

Offering certified courses since 2019

Exemplar Global Recognized Training Provider

Offering certified courses since 2020