With in-depth expertise in European medical device law (MDR, IVDR), many years of sales experience, and a robust international partner network, we support companies in meeting regulatory requirements and successfully entering new markets.
Our advice is practical, confidential and flexible – tailored to start-ups, medium-sized manufacturers and internationally active distributors. We understand the requirements of authorities, the expectations of investors and the reality of the market.
Our team consists of lawyers, regulatory affairs specialists, and sales professionals with a focus on the MedTech, diagnostics, and life science sectors.
We don’t just work with guidelines and paragraphs – we talk to hospital management, pharmacists, government officials and patients. This allows us to understand the actual needs on site – and know how to place medical products where they are needed.
with a regulatory, clinical and economic perspective
for complex international requirements
for medical innovations in Europe, the Middle East and beyond
