Jeppe Larsen

Director of Medical Devices at Danish Medicines Agency

Speaker

Jeppe Larsen, Head of Medical Devices Division, Danish Medicines Agency.

Jeppe Larsen is a prominent figure in the regulatory landscape, currently serving as Head of Medical Devices Division at the Danish Medicines Agency. He is part of the European delegation within the International Medical Devices Regulators Forum (IMDRF) Management Committee, a global initiative dedicated to harmonizing frameworks, definitions, and processes across diverse regulatory systems worldwide. In this role, Jeppe contributes to the advancement of unified global standards in medical device regulation.

Jeppe is the former co-chair of the HMA-EMA Big Data Steering Group, where he represented the Heads of Medicines Agencies (HMA) within the European Union. Collaborating closely with his co-chair, Peter Arlett from the European Medicines Agency (EMA),

Jeppe is actively involved as the Danish representative within several key European expert networks. He is a member of the Medical Device Coordination Group (MDCG), which works to coordinate the implementation of the Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR) across European member states and the European Commission.

Jeppe also contributes his expertise to the Executive group Competent Authorities for Medical Devices (CAMD) network where he is co-chairing together with Dr. Wolfgang Lauer from BfARM, a platform for sharing knowledge and best practices within the MDR and IVDR frameworks.