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United StatesPost Market Surveillance (PMS) under EU MDR 2017/745
16 hours
FREE ON-DEMAND WEBINAR
29th Jan, 2025
3:00 PM - 3:45 PM GMT
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.
Join us on Wednesday, 29th January 2025, from 3pm GMT, where Comply Guru’s Michelle Keane will discuss 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 (Live Event). 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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