Four Considerations when Internal Auditing under the EU MDR Webinar
![Webinar-10-07-2024-internal-auditing-under-the-eu-mdr | Comply Guru Uk](https://complyguru.com/en-gb/wp-content/uploads/sites/5/2024/07/Webinar-10-07-2024-internal-auditing-under-the-eu-mdr.png.webp)
On Wednesday, July 10th 2024, Comply Guru’s Michelle Keane will be hosting a free Webinar on Four Considerations when Internal Auditing under the European Medical Device Regulation (EU MDR 2017/745) from 5-6pm BST.
This Webinar will discuss key topics including:
- How To Approach Internal Audit Scheduling
- Auditing Post-Market Surveillance
- Internal Auditing vs Supplier Re-evaluation incl. Distributor & Importer
- How to Report MDR-based Findings in the Internal Audit Report
- Q&A
This webinar will be recorded and available to registered participants after the event.
Register for FREE to gain access to this Webinar (Live & On-Demand).
Michelle Keane
QA/RA Director
Michelle has a proven track record with more than 20 years’ experience working across both the Medical Device and Biotechnology sectors. Currently, she is a Lead Auditor for an INAB Accredited Certification Body, and an MDR Assessor for a Notified Body in Europe. In addition, she is the Team PRRC Representative for Ireland.