Home / Resources / Medical Device UKCA Series – Part 2
12 Jun 23
In our last post we provided information on UKCA marking (UKCA) for medical devices, what manufacturers need to do since the United Kingdom (UK) left the EU along with the current published timelines for UKCA compliance.
In this post we will provide information on the United Kingdom Responsible Person (UKRP), who needs one, who can act as one and what the UK RP responsibilities are.
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