What is the webinar about?
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.
What will participants gain?
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.
Who should attend?
Anyone involved in transitioning medical devices from the Directives (MDD/AIMDD) to the MDR in the EU.
Choose from one of two sessions on Tuesday 26 March 2024
09.00 - 10.00 GMT Register
16.00 - 17.00 GMT Register
Speakers
Maddalena
Pinsi
Senior Regulatory Lead & Associate Head of Medical Devices Notified Body
Email: medicaldevices@bsigroup.com
Phone: +44 345 080 9000
