As ARTED, we held the panel titled “The Latest Situation in MDR&IVDR Transitions in the EU and Turkey” at the Expomed Eurasia on April 26, 2024 with participants from the Turkish Medicines and Medical Devices Agency and MedTech Europe with active participation from the industry.
The panel moderated by Turkish Medicines and Medical Devices Agency, Medical Device Approval and Clinical Trials Department Head Fatih Topuz which was evaluated in detail under the name of “Document Period Extension in the Transition to MDR in Turkey” presentation by Turkish Medicines and Medical Devices Agency, Medical Device Registration and Coordination Department Head Ömer Faruk Kuru.
Director General Strategies, Special Projects and International Affairs Director of MedTech Europe Jesus Rueda Rodriguez and International Affairs Manager Dario Belluomini also took part in the panel as speakers and expressed their opinions about the future of the system regulating medical device legislation in Europe.