Home Knowledge Act Now to be Ready on Time – Guide to New Classification Rules for In Vitro Diagnostic Medical Devices

Act Now to be Ready on Time – Guide to New Classification Rules for In Vitro Diagnostic Medical Devices

 

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. 

Act Now to be Ready on Time – Guide to New Classification Rules for In Vitro Diagnostic Medical Devices.

 

Contributed by Laura Casey