We support you in the preparation or revision of key documents for CE certification: clinical evaluations, post-market surveillance, risk management, revise for you the technical documentation of your products with regard to the requirements of the Medical Devices Regulation MDR, and accompany you during the transition phase to MDR. On desire, we make also the communication to your Notified Body.

Choose which modules you need. We are happy to support you so that you can successfully launch your products on the market under the MDR.

What can we do for you?

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