On 26.05.2020 ends the three-year transition period of the Medical Devices Regulation MDR, which came into force on 25.05.2017. Depending on the product, this has different consequences for medical device manufacturers. Special attention is also given to the relation of original manufacturers and private label manufacturers. What they all have in common, however, are the increased requirements.

We have adapted our product portfolio especially to the individual needs of medical device manufacturers. Those who prepare early not only ensure the market access of their products, but can also profit from a competitive advantage.

Be always a step ahead with us. We support you:

  • Gap analysis and determination of your individual needs for implementation of the MDR requirements.
  • Preparation of your individual implementation plan.
  • Support during the implementation phase.
  • Communication to the Notified Body.

What can we do for you?

Please contact us without obligation and we will be delighted to advise you on your individual requirements.