Ms. Ajda Mihelčič

Deputy Manager

Publishing Department

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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 medical devices and in-vitro diagnostics industries, so don't miss the webinar!

33 YEARS OF QUALITY

SERVICE IN REGULATORY AFFAIRS

This webinar walks you through key milestones as your company prepares for the IVDR date of application in May 2022, including:

  • IVDR Latest updates: Extended transitional provision for some IVDs
  • Roadmap: The steps to comply with the IVDR by the 2022 deadline

Webinar: Countdown to IVDR Transition

Are you ready for the 26th of May 2022?

Countdown to IVDR Transition

Are you ready for the 26th of May 2022?

FREE!