A regulatory and quality affairs specialist with deep expertise in MDR compliance and international medical device regulations. Anne-Sophie supports companies in navigating complex regulatory landscapes, including FDA, Anvisa, Shonin, and CE marking requirements. She has extensive experience in post-market vigilance, complaint handling, and compliance for medical devices, with technical expertise in radioprotection, medical physics, and X-ray/MRI technologies. With a background in managing multicultural business environments, she is an expert in problem-solving, project management, and regulatory affairs strategy. 

Stijn brings extensive expertise across biotechnology, pharmaceutical chemistry, plant protection products, fertilizers, and food and feed technologies. He is highly skilled in the drafting and prosecution of European and international patent applications and provides strategic advice on filing strategies, patentability assessments, and freedom-to-operate studies. With significant experience in due diligence, he excels at evaluating third-party patent portfolios and optimizing clients’ portfolios for due diligence evaluations. Stijn is also a seasoned advocate in opposition and appeal proceedings before the European Patent Office. Additionally, he is a recognized authority on Supplementary Protection Certificates (SPCs) for pharmaceuticals and agricultural products, qualified to represent clients before the Unitary Patent Office, and a registered Court Expert in Belgium for patent matters, including seizure procedures for suspected patent infringements.