Attorney at Law and Partner
Axon Lawyers, Netherlands
Erik specialises in EU and national legal and regulatory issues relating to medical devices, in vitro diagnostics and software / artificial intelligence and protection of personal data. He is an expert in life sciences regulation at EU and Dutch level, with a focus on contracts, regulatory litigation against competent authorities or notified bodies and M&A. Erik works for the majority of 10 largest medical devices companies in the world as well as many small and middle sized devices companies from all over the world. He contributes to the development of EU medical technology law in advisory committees assisting the European Commission and through his work for the European Parliament. He is author of many publications and of the acclaimed handbook The Enriched MDR and IVDR.
Preconference Workshop: Expand Your Knowledge to Gain Professional Flexibility
Monday, October 6, 2025
8:30 AM - 4:00 PM EST
EU MDR Kick-Off: “The Latest and Greatest News from Europe
Wednesday, October 8, 2025
9:15 AM - 10:30 AM EST
A Lean System to Report Supply Interruptions and Discontinuations (Article 10a in EU, RoW)
Wednesday, October 8, 2025
1:00 PM - 2:00 PM EST
Environmental and EcoDesign Requirements in Europe and Beyond
Wednesday, October 8, 2025
4:30 PM - 5:30 PM EST