The EU-Chaired 23rd session of the IMDRF will gather international professionals in the medical device regulatory field and provide a valuable opportunity for exchange between participating authorities, industry and clinical associations.
Several issues discussed are already being worked on by the CORE-MD consortium such as post-market surveillance, real-world evidence, criteria to evaluation medical devices.
On Day 1, the event will be opened by Andrzej Rys (Principal Scientific Adviser, Directorate-General for Health and Food Safety (DG SANTE), European Commission) and followed by a series of workshops and expert talks.
On Day 2, the opening address will be provided by Stella Kyriakides (EU Commissioner for Health and Food Safety), followed by presentations from regulatory authorities and stakeholder associations globally on latest developments in the field.
The physical meetings planned for these two days in Brussels will make a significant contribution to the work of the IMDRF over the coming year.
To join the discussions and have your say, please follow the registration link to attend.
You can find more information regarding the event on the IMDRF23 website available at www.imdrf2023.com.
· International Cooperation – Medical Devices