La Comisión Europea esta semana hace de anfitrión a IMDRF. El IMDRF es la organización que se ocupa de la armonización de las legislaciones a nivel mundial para productos sanitarios.
nos vemos allí ….
DIA 1 – 25 September 2023
Joint IMDRF / Stakeholder (DITTA-GMTA) Workshop – Specialized Regulatory Pathways
– Opening remarks
– Scene setter – overview of IMDRF foundational pathways
– Devices intended for specific patient populations
– Panel discussion – lessons learned and opportunities for improvement
– Innovative medical devices
– Regulatory toolboxes to foster innovation
DIA 2: 26 Mazo 2023 IMDRF Stakeholder Forum
– Regulatory updates from IMDRF Management Committee and Official Observers including short updates from IMDRF Working Groups
– Regulatory updates from IMDRF Management Committee and Official Observers including short updates from IMDRF Working Groups
– Stakeholders sessions
– Flash panel – exchange of experience and best practices
– Closing remarks
ya participamos en la edición de Bruselas
