Course Area
Availability
Available for 90 days after enrollment
Approximate Course Run Time
1 hour
Continuing Education Units
0.1
Course Fee
No charge
E-learning content is available on demand
Course Details
Overview
After a summary of the (EU) 2023/607 content, the webinar will clarify what are the responsibilities of manufacturers.
We will then explore the potential impact on legacy devices of non-compliance with (EU) 2023/607 conditions and in case of MDR certification refusals.
Key takeaways and learning objectives
Join the webinar to:
- Explore what are the responsibilities of manufacturers in the context of (EU) 2023/607.
- Understand the impact of non-compliance with (EU) 2023/607 conditions in respect to legacy devices and in case of MDR certification refusals.
Presenter information
Speaker - Maddalena Pinsi, Senior Regulatory Lead & Associate Head of Medical Devices Notified Body
