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

July 29, 2020
Partner
Charleen O’Keeffe
Partner
Laura Scott

 

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 

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