MDR

The Medical Device Regulation is comming – together with us you are prepared

Prepare your business and products upfront to the new form of regulation within europe.

Since the beginning of publishing the first drafts we challenged ourselves with the MDR and we are ready to start with the current form the the regulation. By doing this, we can support you during the update-challenge and share our expertise with you.

  • GAP-Analysis
  • Check against new requirements
  • Update of your processes
  • Establish new processes
  • Update of the technical files