medical devices

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

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

Impact of the FDA QMSR on Medical Device Manufacturers

12th Sep, 2024 4:00 PM - 4:45 PM GMT +1 - Michelle Keane

Impact of the FDA QMSR on Medical Device Manufacturers

This is a Free Comply Guru Webinar where the new FDA QMSR Final Rule and its impact on Manufacturers will be discussed by Michelle Keane.

fda final rule manufacturers medical devices qmsr

Overview of Key Changes with MDSAP Audit Approach Version 9

29th Aug, 2024 4:00 PM - 5:00 PM GMT +1 - Michelle Keane

Overview of Key Changes with MDSAP Audit Approach Version 9

This is a Free Comply Guru Webinar covering an Overview of Key Changes with MDSAP Audit Approach Version 9 with Michelle Keane.

auditing mdsap medical devices version 9

Unannounced Audits in the Medical Device Industry

22nd Jul, 2024 5:00 PM - 5:30 PM GMT +1 - Michelle Keane

Unannounced Audits in the Medical Device Industry

This is a Free Comply Guru Webinar on Unannounced Audits with Michelle Keane.

medical devices quality unannounced audit

Four Considerations when Internal Auditing under the EU MDR Webinar

10th Jul, 2024 5:00 PM - 6:00 PM GMT +1 - 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

The Role of the Person Responsible for Regulatory Compliance (PRRC) Webinar

13th Dec, 2023 3:00 PM - 4:00 PM GMT - Michelle Keane

The Role of the Person Responsible for Regulatory Compliance (PRRC) Webinar

This is a Free Comply Guru Webinar on the Role of the Person Responsible for Regulatory Compliance (PRRC) under the EU MDR and EU IVDR with Michelle Keane.

eu ivdr eu mdr medical devices prrc