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UKCA CERTIFICATION REGULATORY CONSULTANCY
A. UKCA Marking for Medical Devices/IVDs:
End-to-end guidance for UKCA marking under UK MDR 2002, ensuring compliance with Great Britain market requirements.
B. UK Responsible Person:
Professional UK Responsible Person services for non-UK manufacturers, ensuring compliance with UK regulatory requirements and acting as your legal representative.
C. MHRA Registration:
Comprehensive support for MHRA registration of medical devices and IVDs, covering all device classes and registration timelines.