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Über mich
I help medical device manufacturers and importers navigate UK MHRA registration, UKCA marking, and UK Responsible Person (UKRP) requirements. I handle documentation preparation, registration submission on the MHRA portal, and guidance on device classification, so your product can legally be placed on the UK market. I also support related EU MDR/CE marking documentation where relevant. Message me with your device type, classification, and current registration status to get started.... Mehr lesen