Comply Guru Webinars

MEDICAL DEVICES

Technical Documentation under the EU MDR 2017/745
Orla Keane
12th Dec, 2024 10:00 AM - 11:00 AM CST - 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.

Impact of the FDA QMSR on Medical Device Manufacturers
Michelle Keane
12th Sep, 2024 10:00 AM - 10:45 AM CST - 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.

Overview of Key Changes with MDSAP Audit Approach Version 9
Michelle Keane
10:00 AM - 11:00 AM CST - 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.

Unannounced Audits in the Medical Device Industry
Michelle Keane
22nd Jul, 2024 11:00 AM - 11:30 AM CST - Michelle Keane

Unannounced Audits in the Medical Device Industry

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

Four Considerations when Internal Auditing under the EU MDR Webinar
Michelle Keane
10th Jul, 2024 11:00 AM - 12:00 PM CST - 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.

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CQI & IRCA Approved Training Provider

Offering certified courses since 2019

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Exemplar Global Recognized Training Provider

Offering certified courses since 2020