medtech

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

29th Jan, 2025 3:00 PM - 3:45 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

MedTech Quality and Regulatory Affairs (QARA) Training Open Q&A

6th Nov, 2024 4:00 PM - 5:00 PM GMT - Eoin Philip Kelly

MedTech Quality and Regulatory Affairs (QARA) Training Open Q&A

Planning ahead on training needs? Looking to budget? Join us on Wednesday, November 6th 2024, from 4pm GMT, where Comply Guru’s Eoin P. Kelly & Michelle Keane will discuss Comply Guru’s MedTech Quality and Regulatory Affairs Training Portfolio. It is a great opportunity to come and ask questions about any course!

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

MedTech Quality and Regulatory Affairs (QARA) Training Open Q&A