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Get UK & EU Authorised Representative in 24 Hours
Euverify provides UK & EU Authorised Representative services for Consumer Products, Electronics, Toys, Cosmetics, Medical Devices, and IVDs. Our platform helps you generate Declarations of Conformity and keep your products legally compliant in Europe.

What is Euverify and How Does It Work?
Everything You Need for Full Product
Safety Compliance
EU & UK Authorised Representative
in 24 Hours
If you do not have a legal presence in the EU or UK, many regulations – including the Toy Safety Directive, Medical Device Regulation (MDR), IVDR, EMC, LVD, RED, PPE, Cosmetics Regulation, and others – require you to appoint an Authorised Representative (EU AR) or UK Responsible Person (UK RP).
Euverify provides an official EU & UK address within 24 hours, which you can immediately use on labels, packaging, documentation, and online listings.




Technical File Builder
Add your products to Euverify through a simple guided flow.
Our system identifies the correct directives and regulations for your product and helps you build, organise, and store your complete technical documentation in one place.
Guided Risk Assessment
Most EU and UK regulations require a documented risk assessment.
Euverify includes a guided template to help you identify hazards, evaluate risks, and apply mitigation steps exactly as required by the EU/UK compliance framework.



Online Marketplace Compliance (Amazon, Etsy, eBay, Shopify)
Ensure your listings meet all safety and information requirements.
Euverify helps you generate the required GPSR compliance documents, including certificates, test reports, and declarations of conformity – everything marketplaces may request to keep your listings active.
10-Year Documentation Storage & Authority Cooperation
EU and UK laws require manufacturers (and AR/RP) to maintain product safety documentation for 10 years.
Euverify stores your technical files securely and handles communication with Market Surveillance Authorities on your behalf – including supporting country-specific language requests.


Support for Product Recalls & Safety Business Gateway Notifications
If a safety issue occurs, the manufacturer and AR/RP must follow formal EU/UK procedures.
Euverify guides you through recalls, corrective actions, incident reporting, and submissions via the EU Safety Business Gateway.
Pay Per Product Type – Not Per SKU
Most products can be registered once per product type, even if you have multiple sizes, colours, or variants.
This makes compliance simple, scalable, and cost-effective. (Some regulated categories – such as certain toys or electronics – may require individual entries.)

Key Compliance Steps
Sign Up & Onboard
Start your free trial and add your manufacturer details.
Appoint an Authorised Representative
Non-UK/EU sellers must appoint an EU/UK Authorised Representative.
Conformity Assessment
Test your product, document compliance, assess risks, and meet GPSR and other regulations.
Affix Markings
Apply required markings (CE, UKCA, EU REP logo) and warnings to your product and packaging.
Add Your Products
List your products, identify applicable regulations, and ensure compliance.
Submit Technical Files
Upload technical files, generate Declarations of Conformity, and prove compliance.
Who Needs UK & EU
Authorised Representatives?
EU and UK regulations require any business without a local physical presence to appoint an Authorised Representative. This applies to:
Why Choose Euverify?
Euverify is a market leader in product safety compliance – offering complete end-to-end support, from UK/EU Authorised Representative services to full technical file and risk-assessment workflows.
What makes us different:
UK & EU Authorised Representative services activated within 24 hours
All-in-one platform for technical files, risk assessments, and traceability
AI-assisted document creation
and compliance guidance
Fast, responsive support from
experienced compliance specialists

Book a Discovery Call
Need help getting started with EU & UK Authorised Representative services?
Book a quick call with our experts to understand what’s required for EU & UK markets and how Euverify can simplify it for you.
Our Pricing
Pricing starts at just
£39/Month
Get complete access to Euverify — your full-service Product Safety compliance platform, including UK/EU Representatives, technical documentation tools, and long-term document storage
What’s Included in Every Plan
- UK & EU Address as Your Official (Representative)
- Communication with Market Surveillance Authorities on your behalf
- 10-Year Secure Document Storage within the EU
- Instant EC & UKCA Declaration of Conformity Generator
- User-friendly dashboard to add and manage your products
- Automatic detection of applicable directives and standards
- Test Report & UKCA and EU Declaration of conformity Certificate
Accepted by : Amazon, Etsy, eBay, Shopify, and major marketplaces
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Frequently Asked Questions
An EU Authorised Representative (EU AR) is a legally appointed organisation based in the EU that represents non-EU manufacturers selling regulated products in the European Union.
You need an EU AR if you manufacture products outside the EU and your items fall under directives or regulations such as GPSR, MDR, IVDR, Toys Directive, EMC, RED, LVD, PPE, Machinery Regulation, Cosmetics Regulation, RoHS, or others.
A UK Responsible Person (UK RP) is the UK equivalent of an EU AR.
If your company is not established in the UK but sells regulated products into the UK market, you must appoint a UK RP to fulfil regulatory obligations and act as the local point of contact.
Typical categories include:
- Electronics and electrical equipment
- Toys and children’s products
- Cosmetics
- Medical devices & IVDs
- Machinery & industrial products
- PPE and safety equipment
- Radios, IoT, wireless products
- Food-contact items
- Household and consumer goods
- Chemical products and aerosols
If the regulation requires a local representative, you must appoint one before selling.
Your AR/RP must:
- Hold and maintain your technical documentation
- Verify regulatory compliance before placing products on the market
- Act as the contact point for authorities
- Assist with inspections, audits, and testing requests
- Handle safety incidents, recalls, and SCMS/SBG notifications
- Ensure your product has correct labeling, CE/UKCA marking, and traceability
- Maintain documents for 10–15 years, depending on regulation
This varies by product category but may include:
- GPSR (EU 2023/988)
- Toy Safety Directive (2009/48/EC)
- Medical Device Regulation (MDR 2017/745)
- IVDR (2017/746)
- EMC Directive (2014/30/EU)
- Low Voltage Directive (2014/35/EU)
- Radio Equipment Directive (RED 2014/53/EU)
- PPE Regulation (EU 2016/425)
- Machinery Regulation (EU 2023/1230)
- Cosmetics Regulation (EC 1223/2009)
- RoHS (2011/65/EU)
- REACH (EC 1907/2006)
- Food Contact Materials Regulation
Euverify supports all major EU and UK regulatory frameworks.
Yes.
Online sales are treated the same as physical sales. Marketplaces require a valid EU/UK contact address and often request AR/RP details, certifications, and safety documentation.
Depending on your product type:
- Technical file
- Declaration of Conformity
- Test reports (EN/ISO standards)
- Risk assessment
- Manufacturing details
- Label artwork with AR/RP address
- Safety data sheets (chemicals/aerosols)
- PIF/CPSR (for cosmetics)
- Device documentation (for medical devices)
Euverify guides you step-by-step.
Activation is usually completed within 24 hours after:
- Sign-up
- Company details submitted
- Digital AR agreement signed
- Documentation uploaded
Your labels will display:
- EU Authorised Representative (Ireland) address
- UK Responsible Person (England) address
Both are exclusive to Euverify clients.
Yes.
All files are securely stored for the full regulatory period (10–15 years).
Authorities can request these at any time, and Euverify manages the communication on your behalf.
Yes.
Your documents are reviewed for completeness, clarity, and regulatory compliance. Missing items are identified and guidance is provided.
Our compliance team:
- Responds directly to authorities
- Provides technical documentation
- Handles safety checks
- Guides you through corrective actions, if needed
- Supports recalls or incident notifications
You will always be kept informed.
Yes.
Euverify acts as Authorised Representative for Class I medical devices and handles:
- EUDAMED registration
- Manufacturer registration
- UDI/traceability
- Document review
- Safety communications
Specialised medical AR services are available.
Yes.
We act as Responsible Person for cosmetics and handle:
- CPSR
- PIF
- CPNP submissions
- Label review
- Safety documentation
- Post-market surveillance
CE marking applies to the EU market.
UKCA marking applies to the UK market.
Some products require both, depending on where you sell.
Euverify assists with both regulatory pathways.
Yes, you may choose AR-only service.
However, most clients prefer the full platform because it includes dashboards, automated compliance flows, file management, and templates.
Yes.
Our service supports multiple brands, categories, and product families within your account.
You must notify us.
A revised technical file or updated documentation may be required depending on the change.
Yes — that is exactly who AR/RP services are designed for.
We support businesses from the US, China, UK, Switzerland, UAE, Australia, India, and more.
No.
Subscriptions can be cancelled anytime, and there are no minimum-term commitments.
Yes.
You may choose:
- EU AR only
- UK RP only
- Both together (recommended for global brands)
We support:
- Consumer products
- Electronics
- Toys
- Cosmetics
- Medical devices
- PPE
- Food-contact materials
- Machinery
- DIY and tools
- Sports and outdoor
- Household items
- Industrial equipment
Yes — this is part of the service.
Your packaging can show our EU or UK address as required by law.
All files are encrypted and stored in secure EU-based systems.
Access is restricted, and compliance with GDPR/UK GDPR is guaranteed.