The reform of the EU MDR

The European Union Medical Device Regulation (EU MDR) continues to shape the way medical technologies are developed, evaluated and brought to market across Europe. While the regulation was introduced to strengthen patient safety and improve clinical evidence requirements, its implementation has also presented significant challenges for innovators, manufacturers, healthcare providers and regulatory bodies.

Join us at the ATU iHub for an engaging roundtable discussion exploring the ongoing reform of the EU MDR. This session will bring together industry leaders, entrepreneurs, regulatory experts and clinicians to examine the current landscape, discuss proposed changes, and consider how reforms may impact innovation, market access and competitiveness within the European medical technology sector.

Through open discussion and shared perspectives, participants will have the opportunity to explore practical experiences, identify emerging opportunities and challenges, and contribute to a broader conversation on the future of medical device regulation in Europe. This roundtable aims to foster collaboration and provide valuable insights for companies navigating an evolving regulatory environment.

Thursday 12th November 6 – 8 pm at @ ATU iHub Galway. 

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Event Details

• ✅ Free to attend

Terms and Conditions

ATU, ATU Innovation Hubs and M.Sc. in International Medical Technologies, Innovation and Development are asking you to register in advance for this event. We will ask you for your name and email address so we may contact you after the event for feedback. We would also like to retain your email address to contact you in the future with news and information on future events. 

If at any time you wish to stop receiving these updates from us, please contact us at: turlough.rafferty@atu.ie.  We will not share your information with any third parties.

By booking to attend this event, you agree to these terms and conditions.