DON’T LET THE IVDR
TAKE YOU BY SURPRISE
The deadline to fully comply with the In Vitro Diagnostic Regulation (IVDR) is just around the corner.
Are you ready?
Download
EU IVDR Timeline
There are several important dates to remember during
the implementation of the new regulation.
May 26, 2017
EU IVDR published and entered into force
NOV 26, 2017
Notified bodies may apply for designation according to the EU MDR
May 26, 2022
EUDAMED goes live
MAY 26, 2022
IVDR Date of Application. EC Certificates of Conformity issued before May 26, 2017 will expire. Certificates issued under the IVDD after May 26, 2017 are valid for an additional 2 years
MAY 26, 2024
All devices placed on the market must conform with IVDR. EC Certificates issued after May 26, 2017 become void
MAY 26, 2025
All devices with IVDD certificates can no longer be sold or put into service
EU IVDR RESOURCES
To better understand the requirements of the
European Union's In Vitro Diagnostics Regulation and the impacts on language, download and read our other resources on the EU IVDR.
Register once, and get access to all our resources.
Get in touch with us for more information.
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touch
For more information on how Argos Multilingual can support you and your business with the
EU IVDR directive and its requirements, please reach out to us by filling in this form.