Date: 14 July, 2025
Location: Abbott Conway Park, Illinois, USA
Language: English
Introduction
Eight years after the official publication of the EU Medical Device Regulation (MDR) and the In Vitro Diagnostic Regulation (IVDR), the European healthcare system continues to face significant challenges in achieving full implementation. Despite ongoing efforts to support compliance and uphold patient safety, stakeholders such as manufacturers, notified bodies, and competent authorities are still navigating obstacles to regulatory alignment.
In this expert presentation, Gert Bos (Qserve Group) and Dr. Bassil Akra (AKRA TEAM) will offer a comprehensive overview of the current regulatory landscape in the EU. They will explore the persistent issues affecting implementation, assess proposed solutions, and share their perspectives on both immediate corrective actions and long-term strategies.
Attendees will gain a deeper understanding of the evolving regulatory environment and its implications for the medical device and in vitro diagnostic sectors across Europe.
For more information and to register, visit the RAPS event website.
Qserve Attendee