Medical Device Company Approved to Prolong MDR Transition Until 31. December 2028

CS MEDICA (“CS MEDICA or The Company”) a medical device manufacturer with leading CBD technology, has been approved by regulatory authorities to extend the transition period to the Medical Device Regulation (MDR) until end 2028. The extension comes as a relief to the Company and many other researchers and healthcare professionals concerned about the impact of the strict regulatory requirements on the availability of medical devices. The MDR, which came into effect in May 2017, replaces the Medical Device Directive (MDD) and imposes stricter regulations on medical device