EU Medical Device Regulations - Timelines and Article 120

During this module we will look at the transition and overall timeline in context with the IVDR and explain some of the technicalities of what products can or cannot be placed on the market after the May deadline.

We will look at the hard deadline and the soft transition, including
Reclassification
Certificate expiries
Significant changes
Placing items on the market
 eCommerce situations

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What's included?

  • 1 Module
  • 1 Certification

Mobile Compatible

As well as using a desktop or laptop, you can run the course
on mobile devices such as; phones, tablets and e-Readers.

Bite Size Learning

A Short video presentations, split onto modules to facilitate easy learning.
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