UKCA Marking for Medical Devices in Algeria – Operon Strategist


UKCA Marking is mandatory for medical devices and IVDs sold in Great Britain, replacing CE marking after Brexit. Algerian manufacturers must comply with UK MDR 2002, prepare technical documentation, and register with MHRA. Operon Strategist guides companies through conformity assessment, QMS alignment, and UK Responsible Person (UKRP) appointment. This ensures smooth regulatory compliance and faster market entry into the UK.



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