When choosing a UK Responsible Person (UKRP) for your medical devices, experience is one of the most crucial factors to consider. An experienced UKRP understands the complexities of UK medical device regulations, including UK MDR 2002, and is well-versed in the evolving post-Brexit compliance landscape. They can efficiently handle responsibilities such as verifying technical documentation, liaising with the MHRA, managing post-market surveillance obligations, and ensuring timely incident reporting. An experienced UKRP also provides strategic regulatory guidance, reducing the risk of non-compliance and market delays. Their industry knowledge allows them to anticipate regulatory changes and advise manufacturers proactively, safeguarding both business continuity and product availability in the UK market.