UK & EU Market Access

Your UK Responsible Person, for manufacturers selling into Britain

We act as UK Responsible Person for medical device and cosmetics manufacturers based outside the UK, and support food supplement importers and EU GPSR compliance — so your products can legally reach UK and EU customers.

UK MDR 2002 & UKCA UK Cosmetics Regulation 15+ Years Experience Clients Worldwide

Why appoint us as your UKRP

1 A genuine UK-based point of contact, required by law for GB market access
2 Direct experience preparing MHRA and OPSS/SCPN submissions
3 One team covering medical devices, cosmetics, supplements and GPSR
4 Straightforward guide pricing, no hidden fees
15+
Years' Regulatory Experience
4
Compliance Services Under One Roof
100%
UK-Based Team
48hr
Typical Enquiry Response Time
What We Do

Four ways we help you reach UK & EU customers

If you manufacture outside the UK and want to sell medical devices, cosmetics, food supplements, or general consumer products into the UK or EU, one of these applies to you.

Medical Devices UKRP

UK Responsible Person duties for Class I, IIa, IIb, III and IVD devices, plus MHRA registration and technical file review.

Learn more →

Cosmetics UKRP

Responsible Person appointment, SCPN notification, CPSR reports, PIF maintenance and labelling compliance.

Learn more →

Food Supplements

UK import and compliance support: permitted-ingredient checks, label review, and Food Business Operator guidance.

Learn more →

EU GPSR & General Products

Compliance advisory for the EU General Product Safety Regulation, plus support arranging your EU Responsible Person.

Learn more →
Why It Matters

No UK Responsible Person, no UK market

Since 1 January 2021, medical devices placed on the Great Britain market by a manufacturer based outside the UK must have a UK Responsible Person registered with the MHRA. Cosmetics sold in the UK need a UK-based Responsible Person too, under the UK Cosmetics Regulation. Without one, your products simply cannot legally be placed on the market — whatever platform or distributor you're using.

We register as your named UK Responsible Person with the relevant authority
We hold and maintain the technical documentation required in the UK
We act as the first point of contact for UK regulators and market surveillance
We keep you informed of regulatory changes that affect your product
Check What You Need →
Our Process

From first enquiry to compliant market access

01

Free consultation

We review your product, target market and existing documentation, and confirm exactly what's required.

02

Document & gap review

We check your technical file, labelling and safety documentation against UK (and where relevant EU) requirements.

03

Registration & appointment

We register as your UK Responsible Person and complete the relevant MHRA or OPSS/SCPN submission on your behalf.

04

Ongoing support

We stay on as your named UK contact, handling regulator correspondence and flagging any regulatory changes.

Which Service Do I Need?

Find the right compliance route for your product

Product typeApplicable regimeUK-based representative required?We can act as your representative?
Medical devices & IVDsUK MDR 2002YesYes
CosmeticsUK Cosmetics RegulationYesYes
Food supplementsUK food law (no RP scheme)No formal roleImport & compliance support
General consumer products into the EUEU GPSRYes (EU-based)Advisory & referral only

Not sure which row applies to you? Tell us about your product and we'll confirm in writing, free of charge.

Ready to access the UK market?

Book a free, no-obligation consultation and we'll tell you exactly what's required for your product.

Book Free Consultation