Ven a estas jornadas donde se abordan los temas mas debatidos de los reglamentos MDR e IVDR por expertos europeos, con la participación de la Comisión Europea, Medtech, EAAR, Qserve, Emergo, Obelis, Axon, Qarad, Informa y Tecno-med.
Claire Murphy presentará en la sesión 2 del 2 de febrero a las 12h el tema de «National Requirements Additional to MDR»
In this 7th edition of the Conference you will have the opportunity to gain a better understanding on the new European regulations on medical devices. Additional regulations (implementing acts) of the Medical Device Regulation and new guidance are issued frequently adding to the complexity. It is important to keep up-to-date with the fast evolving compliance scene.
This event addresses to all those involved in the medical device field worldwide, such as Medical Device Companies, R&D and QA personnel, CEOs / CROs / CRAs, Regulatory Affairs Specialists, Research facility managers, Pharmaceutical Company representatives and Start-Up Companies.
In conjunction with EAAR (European Association of Authorized Representatives), our excellent panel of experienced professionals in this field will once again ensure a conference of noteworthy quality.
RMD2023 gives the best opportunity for sponsors and exhibitors to network face-to-face with a target audience of medical device regulation professionals.
We look forward to seeing you at the 7th EAAR Annual Conference on New Medical Device Regulations (RMD2023) in the beautiful and historical city of Brussels.
Este es el programa