Find a UK Responsible Person (UKRP)
Post-Brexit, non-UK manufacturers placing regulated products on the GB market must appoint a UK-established Responsible Person under UKCA marking requirements, UK MDR 2002, UK RED and other UK regulations. Submit one request — ECP connects you to UK RP providers with the coverage you need.
Who needs a UK Responsible Person?
Any manufacturer established outside the United Kingdom who places regulated products on the GB market must appoint a UK Responsible Person (UKRP). This is a post-Brexit requirement — your EU Authorised Representative cannot serve as UKRP.
| Regulation | Requirement | Scope |
|---|---|---|
| UK MDR 2002 (as amended) | Mandatory — MHRA registration required | All medical devices from non-UK manufacturers |
| UKCA marking (general products) | Required for UKCA-marked products | Products requiring UKCA conformity marking |
| UK Radio Equipment Regulations 2017 | Required for non-UK manufacturers | Radio and telecommunications equipment |
| UK PPE Regulations 2018 | Required for non-UK manufacturers | Personal protective equipment |
| UK Toys (Safety) Regulations 2011 | Required for non-UK manufacturers | Toys and children's products |
MHRA medical device registration is mandatory before placing devices on the GB market. The UKRP must register the manufacturer and devices in the MHRA database. Non-compliance can result in products being refused entry or withdrawn from the UK market.
What the UK Responsible Person does
- Acts as the UK-established legal contact for the manufacturer with MHRA and other UK authorities
- Registers the manufacturer and their products in the MHRA medical devices database (for medical devices)
- Holds copies of technical documentation, Declaration of Conformity, and other required documents
- Cooperates with MHRA on market surveillance inquiries, vigilance, and safety actions
- Coordinates product recalls and field safety corrective actions in the UK market
- Ensures UKCA marking documentation is current and correct
- Named on the product label or packaging as the UK RP
Documents and information typically required
- Product description, intended use and applicable UK regulations
- Existing EU CE marking certificates (if applicable)
- Current UK MDR risk class (Class I, IIa, IIb, III) for medical devices
- Number of distinct product models requiring UKRP coverage
- Target launch date or current UK market presence status
- Any existing MHRA registration numbers
Many providers offering EU Authorised Representative services also offer UK RP through affiliated UK-established entities. A combined EU AR + UK RP package from one provider reduces administrative overhead and cost.
Related services
| Service | Description |
|---|---|
| EU Authorized Representative (EC REP) | Mandatory EU AR for non-EU manufacturers under MDR, IVDR, RED, LVD — separate from UK RP |
| PRRC Services | Person Responsible for Regulatory Compliance under MDR/IVDR Art. 15 |
| Swiss FADP Representative | Swiss data protection representative — another separate jurisdiction |
| Compare EC REP Providers | Compare EU AR providers including those with UK coverage |
Ready to Start?
Non-UK manufacturers placing UKCA-marked products on the GB market must appoint a UK Responsible Person. Submit one request — ECP matches you to UK RP providers for medical devices, radio equipment and other regulated products.
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