Mr. Erik specialises in EU legal and regulatory frameworks for medical devices, digital health technologies, pharmaceuticals, and life sciences, with distinctive expertise in AI, software, in vitro diagnostics and personal data protection.

As a multilingual legal expert with extensive experience at the European Commission and several leading international law firms, he provides strategic counsel on complex regulatory and legal matters across medicinal products, medical devices, biotech and in vitro diagnostics sectors. His clients include the largest medical technology manufacturers and pharmaceutical companies in the world to start-ups as well as EU institutions, national governments and industry associations.

Erik’s expertise spans regulatory advice and litigation, commercial contracts, M&A transactions, and comprehensive regulatory strategy for medical technology, pharmaceutical, biotech and in vitro diagnostic enterprises.

An internationally recognised authority in life sciences regulation, Erik actively contributes to EU and national law and policy development through specialised committees at both national and EU levels. He is strategic advisor on law and policy development in medical technology for several EU institutions, governments and industry associations.

He serves as an arbitrator in medical device-related disputes and is regularly retained as an external expert in litigation.

Leveraging professional experience in Brussels, Amsterdam and Stockholm, Erik offers nuanced legal insights across multiple jurisdictions. Proficient in Dutch, English, French, German, Spanish and Swedish, he provides strategic, sophisticated, cross-border regulatory  and legal guidance for complex medical technology and life sciences challenges.