New procedures for medical devices from September
The technical oversight responsibilities for medical diagnostic devices will be transferred to the National Agency for Medicine and Health Products starting from September 1, 2026. The agency has called on suppliers to submit their documents to the relevant departments, emphasizing that the current evaluation procedures and standards will remain unchanged. The agency is committed to ensuring the continuity and efficiency of the service, while informing stakeholders of any future measures that may be implemented. Up to now, the Medical Biology Laboratories Unit of the Ministry of Health has been responsible for overseeing these tasks.
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