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Post Market Surveillance (PMS) under EU MDR 2017/745
16 hours
€995.00
FREE ON-DEMAND WEBINAR
29th Jan, 2025
5:00 PM - 6:30 PM ETT
Post Market Surveillance under the EU MDR – Challenges and Best Practices
Post Market Surveillance (PMS) under the EU Medical Device Regulation (EU MDR 2017/745) is an area of huge interest to Manufacturers looking to do business in Europe.
On Wednesday, 29th January 2025, Comply Guru’s Michelle Keane discussed the challenges and best practices for Post Market Surveillance (PMS) under the EU Medical Device Regulation (EU MDR 2017/745).
This Webinar will discuss key topics including:
- Lack of Real-World Data
- Resource Constraints
- Use of Digital Tools and Automation
- Ensuring Cross-Functional Collaboration
- Auditing Post Market Surveillance
Register for FREE to gain access to this Webinar (On-Demand for 30-days). Please note that registration is required to join.
Register for free
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.
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