The 9th EAAR Annual Conference on New Medical Device Regulations (RMD 2025) took place in Brussels, Belgium, on 24-25 February 2025, featuring speakers from across the MedTech industry, including regulators and notified bodies.Organized by the European Association of Authorised Representatives (EAAR), the conference served as an inclusive platform for all stakeholders across the both medical device and IVD landscapes.

With a dedicated focus on the challenges faced by manufacturers and other stakeholders in meeting the EU MDR and IVDR requirements, the event invited attendees to delve into the European regulations, fostering insightful discussions on pivotal facets of these ever-evolving regulatory frameworks.

Donawa Lifescience President, Maria E. Donawa, M.D., spoke on the second day, covering the topic ‘Strategic Approaches to Clinical Data Requirements in the EU and US’.

The conference also provided opportunities for one-on-one meetings with the speakers and event organisers.