Our conference serves as an inclusive platform for all stakeholders across the medical and IVD medical devices landscape. With a dedicated focus on the challenges faced by manufacturers and other stakeholders in embracing the EU MDR and IVDR, the event holds promise for all attendees, irrespective of their diverse backgrounds. This occasion invites you to delve into the depths of European regulations, fostering insightful discussions on pivotal facets of these ever-evolving regulatory frameworks.

Spanning topics from the divergence in national implementation of the regulations across Europe to cutting-edge regulatory topics concerning AI, clinical evaluation, UDI, post-market surveillance, and technical documentation, the Conference offers an all-encompassing journey. Covering the European Union, United Kingdom, and Switzerland, the Event is poised to unravel a myriad of subjects that are of paramount importance.

The RMD Conference promises to be a momentous juncture for combining diverse actors and subjects within the compliance landscape. EU officials, Manufacturers, competent authorities, notified bodies, and business associations will converge, igniting a collective dialogue that holds the potential to shape the future of the industry.

We look forward to meeting you at RMD2025 in Brussels.

Sincerely,

Ludger Möller

EAAR Chairman, President, Medical Device Safety Service, Germany
Conference Chair