ARTED visited Turkey Medicines and Medical Devices Agency Sectoral Services Department Head

ARTED Regulation Working Group President Burak Kaptan, Vice Presidents Serlin Ceran, İrem Çokgez Göçer, ARTED Secretary General Elif Özman Pusat, Ankara Representative Semih Yılmaz visited the Head of Medical Device Registration Coordination Department of the Turkish Medicines and Medical Devices Agency Ömer Faruk Kuru on November 29, 2024. During the meeting; Medical Device Regulation (MDR) & In Vitro Diagnostic Medical Device Regulation (IVDR) standardizations regarding products with extended transition periods, supply interruptions and terminations to be implemented in the EU, future talks and plans of ÜTS and customs systems, and rejection data regarding ÜTS product applications from our members were conveyed. At the end of the meeting, it was stated that the contributions that can be provided as ARTED and that our regular visits will continue in the following processes.