In November 2024, RADEX, in collaboration with XENOPHARMA, delivered a specialized training course to the Kurdistan Medical Control Agency (KMCA-Erbil) titled “EU MDR Medical Devices: Navigating the Regulatory Landscape.” This focused program was tailored specifically for KMCA’s dedicated team.
This intensive program was meticulously crafted to equip the KMCA Staff with the in-depth knowledge and practical skills necessary to seamlessly navigate the complex regulatory environments of both the European Union’s Medical Device Regulation (EU MDR) and Saudi Arabia’s medical device regulations.
RADEX was delighted to conduct this course in cooperation with XENOPHARMA, and we extend our sincere appreciation to the KMCA-Erbil inspection and registration departments for their active engagement and commitment to advancing regulatory excellence.