Medical devices present a wide-ranging field, and their specific medical purposes vary immensely. It requires two European Regulations – the Medical Device Regulation (MDR) and the In Vitro Diagnostic Device Regulation (IVDR) specifically for medical devices used for in vitro diagnosis – to ensure products meet the standards of quality, safety, and performance.

Adding the fact that a medical device can be anything from an instrument, appliance, or software to an implant or a reagent, it poses a particular challenge to find your way around in this sector.

We support you along the entire medical device life cycle:

From design and development to registration and beyond: We always consider your individual needs, challenges, and potential – and round them off with our knowledge of medical devices, pharmaceuticals, and combination products. Combined with efficient business concepts, we can provide a holistic approach throughout the entire value chain of products and services.