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Chi sono
I help medical device companies achieve smooth UK market entry through accurate MHRA registration and regulatory compliance support. With experience handling UK MDR submissions for medical devices, IVDs, and surgical products, I assist manufacturers, importers, and distributors with device classification, GMDN selection, DORS submissions, technical document review, and UK Responsible Person guidance. My goal is to simplify the registration process, reduce delays, and ensure your products meet UK regulatory requirements efficiently and professionally... Continua a leggere