UKRP Services for Foreign Manufacturers | |
UKRP services for foreign manufacturers are essential for ensuring that medical devices, in vitro diagnostic devices, and other healthcare products can legally be placed on the UK market following Brexit. As per the UK Medical Device Regulations, any manufacturer based outside the United Kingdom is required to appoint a UK Responsible Person (UKRP) who will act on their behalf within the UK. This representative takes on crucial regulatory responsibilities, including registering the manufacturer’s devices with the Medicines and Healthcare products Regulatory Agency (MHRA), maintaining the technical documentation, and ensuring the manufacturer meets all applicable regulatory requirements. The UKRP also serves as a primary contact point for the MHRA and cooperates with the agency during inspections, product recalls, and safety concerns. For foreign manufacturers aiming to maintain uninterrupted access to the UK healthcare market, partnering with a reliable and experienced UKRP ensures regulatory compliance, market continuity, and timely communication with national health authorities, making it a vital element in a successful market access strategy. Read more: https://www.ukrpservices.com/ukrp_services ![]() | |
Target State: All States Target City : Kavaratti Last Update : Jun 10, 2025 6:10 AM Number of Views: 17 | Item Owner : ukrpservices Contact Email: Contact Phone: (None) |
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