MHRA Registration Specialist UK Medical Device UKCA Compliance Support
Regno Unito
Inglese, Spagnolo, Francese, Tedesco, Italiano
Alcune informazioni sono riportate in lingua inglese.
Chi sono
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.... Continua a leggere