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MEDICAL DEVICES
Navigating the FDA QMSR Transition: A Practical Gap Analysis Approach
This is a Free Comply Guru Webinar where Navigating the FDA QMSR Transition: A Practical Gap-Analysis Approach will be discussed by 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.
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.
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.
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.
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!
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.
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
This is a Free Comply Guru Webinar on Key Considerations when Internal Auditing under the EU MDR with Michelle Keane.
