medtech

10th Mar, 2025 3:00 PM - 3:45 PM GMT - Michelle Keane

How to Prevent Weak CAPA Investigations

This is a Free Comply Guru Webinar where How to Prevent Weak CAPA Investigations will be discussed by Michelle Keane and special guest Jackie Torfin.

auditing capa fda qmsr iso 13485 medical devices medtech

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

29th Jan, 2025 5:00 PM - 6:30 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

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!

medical devices medtech open day qara training

How to Prevent Weak CAPA Investigations

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

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