In advance of the In Vitro Diagnostic Medical Devices Regulation (EU) 2017/746 (the IVDR) becoming fully applicable on 26 May 2022, we outline the key changes to the classification of in vitro diagnostic medical devices (IVDs).
In this briefing we cover:
- Classes of IVDs
- Classification Rules
- Impact of Classification Changes
- Device Identification
Click here or on the image below to download our full briefing.
Contributed by Laura Casey
