EU IVDR now applies in Europe:

What should IVD manufacturers do to comply? 

In May 2022, the new In-Vitro Diagnostics Regulation became fully applicable in the European Union. This implementation has brought a significant amount of challenges in the requirements to market products on the EU market.

If you are unsure of how you should now proceed in order to import new devices, or maintain the previous ones in the European territory, this webinar is what you were looking for.

Our experts will be discussing: 

  • Which are the steps to follow;
  • How to determine the status/class of your device, and what are the related implications;
  • The Authorized Representative's role in the review process

Access the webinar for FREE:



Complying with the EU Market Regulations can be a daunting task to undertake on your own. Make sure you get all the information you need. 

We bring our experience and knowledge in the cosmetics regulatory field, so don't miss the webinar!


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Davide Turchi

Regulatory Affairs Manager

Ajda Mihelčič

Publications Manager

June 30, 2022

11:00 CET // 17:00 GMT+8