Annette van Raamsdonk, LL.M. is a senior Quality and Regulatory Affairs leader with extensive experience in the European medical device and in vitro diagnostics sector. As Manager Quality & Regulatory Affairs Program at Emergo by UL, she leads strategic regulatory programs, Authorized Representative services, and cross-functional initiatives in a complex and highly regulated environment. She combines deep legal and regulatory expertise with strong leadership, sound judgement, and the ability to translate complex requirements into practical, high-quality solutions for manufacturers, Economic Operators (EOs), healthcare institutions and internal teams. Annette is recognized for her professionalism, integrity, and ability to build trusted relationships across industry, Notified Bodies (NBs), Competent Authorities (CAs), professional associations, and European institutions, such as the European Commission. Her broad European MedTech network enables effective stakeholder engagement, early insight into regulatory developments, and constructive collaboration on strategic issues.