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Buyer's guide

EU Authorised Representative Services for Non-EU Manufacturers

Short answer: Non-EU manufacturers selling products or processing personal data in the EU are often legally required to appoint an EU authorised representative. This obligation arises under regulations such as the General Product Safety Regulation, Machinery Regulation, and GDPR Article 27. Several providers—including REP27, Cleo Labs, and others—offer these services, each with distinct pricing and included features.

Updated · 16 sources checked

Providers compared

ProviderEstablished inPublished priceWhat the price includesBest for
REP27Czech Republic (EU)from €190/year (GPSR), €290/year (GDPR), €690/year (cosmetics), €1,490/year (AI Act Art. 54)Written mandate, certificate, public verification, address for labels, unlimited products (GPSR plans), 24h human review, one contract/invoice for EU & UK if neededBrands needing fast, verifiable EU representation for GDPR, product, cosmetics, AI, and more
Cleo LabssourceLikely United KingdomFrom €1,500 per year per product categoryMandate, label contact, documentation retention, answers to authorities, regular product checks, expert review, monitoring, corrective action supportCompanies needing ongoing compliance support and product checks
EaseCertsourceAustria (EU)€1,050 one-time feeOnboarding, compliance material review, document verification, technical documentation checks for GPSRManufacturers seeking a one-off compliance check and setup
Conformity PointsourceUnited KingdomYear 1: €199/product; Renewal: €119/product/yearMandate, basic technical file, label details, document retention, authority requestsSmall product lines needing low annual cost per product
ProductIPsourceNetherlands (likely)Setup: €1,950; Annual: €2,150; €240/hour for issuesEU AR services with technical file review, ongoing representation, hourly support for AR issuesComplex portfolios needing documentation and ongoing support
Authoriseme.eusourceAustria, Spain, Germany, Czech Republic, SlovakiaFrom €199/year (packaging); WEEE & Batteries: €150–870/year depending on country/packageAR service for packaging, WEEE, batteries, tires, annual and one-time fees by category/countryEnvironmental compliance for packaging, batteries, WEEE

Prices as published on each provider's website on 31 October 2026, excluding VAT unless stated. Each row links to its source.

What the Law Requires: Article Numbers and Obligations

EU law imposes clear obligations on non-EU manufacturers and service providers to appoint an authorised representative (AR) established within the European Union. This requirement is not limited to a single regulation, but spans several key legal frameworks, each with its own scope and triggers:

Failure to comply can result in fines, product withdrawal, or marketplace bans. The AR acts as the first point of contact for EU authorities and consumers, and must retain technical documentation and declarations of conformity for at least 10 years, as required by CE marking and product safety rules.

Key takeaway: If you are a non-EU manufacturer or service provider selling regulated products or processing EU personal data, you likely need to appoint an EU AR before entering the market.

How to Choose an EU Authorised Representative

Choosing the right EU authorised representative is crucial for compliance, smooth market access, and risk management. Here are the most important factors to consider, based strictly on published provider data:

ProviderIncludedNot IncludedExtra Fees
REP27Mandate, certificate, public verification, unlimited products (GPSR), 24h reviewLegal advice, technical file creationOn request
Cleo LabsMandate, contact, documentation, product checks, expert reviewOn requestOn request
EaseCertOnboarding, review, verificationOngoing AR supportOn request
Conformity PointMandate, file, label, retentionOngoing support (beyond basic)On request
ProductIPMandate, technical file reviewHourly support for issues€240/hour
Authoriseme.euMandate for packaging, WEEE, batteriesOther product typesCountry/package dependent

Always request a full list of included services, ask about hidden costs, and check if the provider's scope matches your products and markets.

What the Price Really Includes (and Hidden Costs)

Published prices for EU authorised representative services can be misleading if you do not read the fine print. Here’s how the main providers compare based on their public information:

Hidden costs to watch for:

Always request a complete price breakdown and clarify what is included before signing.

How Appointment Works: Step-by-Step Process

The process of appointing an EU authorised representative is straightforward, but must be done carefully to ensure compliance and avoid delays. Here’s a step-by-step guide based on provider practices and legal requirements:

  1. Identify your obligations: Determine which EU regulations apply to your products or services (e.g., GPSR, machinery, cosmetics, GDPR, AI Act).
  2. Collect compliance documents: Gather technical files, declarations of conformity, and any supporting safety or data protection documentation.
  3. Choose a provider: Compare published prices, included services, and scope. Verify that the provider is established in the EU and covers your product type.
  4. Submit your file: Provide company and product details, compliance documents, and any required questionnaires. REP27 reviews files within 24 working hours; other providers may vary.
  5. Provider review: The provider checks your file for completeness and may request clarifications or additional documents.
  6. Mandate signature: Once approved, the provider signs the written mandate. REP27 issues a signed letter, certificate with QR code, and public verification code.
  7. Update labels and documents: Add the AR’s name and address to your product labels, packaging, website, and privacy notices as required by law.
  8. Verification: Authorities and marketplaces can check your AR’s status via public registers or verification tools (offered by REP27 and some others).
  9. Ongoing compliance: Keep your documentation up to date, notify your AR of incidents, and respond promptly to authority requests.

Checklist for buyers:

  1. Identify the relevant EU regulation(s) for your products/services.
  2. Collect all technical and compliance documentation.
  3. Shortlist providers based on scope and price.
  4. Request a sample mandate and certificate.
  5. Submit your application and documents.
  6. Receive and implement the AR appointment.
  7. Update all labels, packaging, and websites with the AR’s details.
  8. Retain all compliance documents for at least 10 years.

Risks and Fines for Non-Compliance

Failing to appoint an EU authorised representative when required exposes non-EU manufacturers to significant legal and commercial risks. Here’s what can happen, based on official sources and regulations:

Examples:

Appointing a reputable AR with public verification and clear documentation is the simplest way to avoid these risks.

Decision Matrix: Do You Need an EU Authorised Representative?

If you are …You need …You do not need it if …
Non-EU manufacturer selling B2C in EUEU AR for GPSR, machinery, cosmetics, etc.Products are not consumer-facing or are only for export outside EU
Non-EU SaaS or cloud provider handling EU personal dataGDPR Article 27 representativeProcessing is occasional, low risk, or only for non-EU persons
Non-EU Amazon/Etsy/eBay sellerEU AR for product safety and labellingMarketplace acts as importer and assumes responsibility (rare)
Non-EU B2B exporter (industrial)AR if products are regulated (e.g., machinery, medical devices)Products not covered by EU regulations
Non-EU manufacturer of packaging, batteries, WEEEAR for environmental compliance (Authoriseme.eu)Products are not placed on the EU market
EU-based manufacturerNot requiredAlready established in the EU

Use this matrix to quickly check if your business needs an EU AR. When in doubt, consult the relevant regulation or ask the provider for a compliance check.

What Providers Usually Do Not Say

Always ask for a full contract, list of included services, and details on exclusions or extra fees before appointing an AR.

Realistic Scenarios: Which Obligation Applies?

In each scenario, the simplest compliant route is to:

  1. Identify the relevant regulation (GDPR, GPSR, cosmetics, etc.).
  2. Collect required documentation (privacy notice, technical file, product information file).
  3. Appoint an AR with public verification and clear scope.
  4. Update all labels, websites, and documentation as required.

Failure to follow these steps can result in fines, product withdrawal, or marketplace bans.

When you do not need this

Frequently asked questions

Who needs an EU authorised representative?

Any non-EU manufacturer placing regulated products (such as consumer goods, machinery, cosmetics, medical devices) on the EU market, or processing EU personal data (GDPR), usually needs an EU authorised representative. The requirement depends on the specific regulation and product type.

What does an EU authorised representative do?

The AR acts as your legal contact in the EU, keeps compliance documentation, responds to authorities, appears on product labels, and may notify authorities of incidents. The AR does not manufacture or import products but ensures regulatory obligations are met.

How quickly can I get appointed?

REP27 reviews and signs most designations within 24 working hours after receiving all required information. Other providers may take longer, especially if document review or technical checks are involved. Always confirm expected timelines before committing.

Can I use the same AR for multiple products?

Yes, if the provider allows it. REP27 covers unlimited products on its GPSR plans. Some providers charge per product or category, so check their pricing structure and contract terms before appointing.

What documents do I need to appoint an AR?

Typically, you need your company details, product information, compliance documentation (such as declarations of conformity), and sometimes technical files or safety data. The AR will review these before signing the mandate and may request clarifications.

Are there ongoing obligations after appointment?

Yes. You must keep compliance documents up to date, notify your AR of incidents, and update labels or privacy notices if details change. The AR may request updated documentation or information during the contract period.

What happens if I do not appoint an AR?

If you do not appoint an AR when required, your importer or distributor becomes legally responsible. Authorities may fine you, order product withdrawal, or ban your products from marketplaces. Non-compliance can also damage your reputation.

Can I change my AR later?

Yes, but you must update all labels, documentation, and notify authorities or marketplaces as needed. Some providers may require notice or charge a transfer fee. Always check contract terms before switching.

Are ARs liable for product defects or incidents?

ARs are responsible for regulatory compliance, not for manufacturing defects. However, they may need to notify authorities of incidents and cooperate in corrective actions. Liability limits and exclusions vary by provider and contract.

Is public verification of my AR appointment important?

Yes. Marketplaces and authorities may check your AR’s details. Providers like REP27 offer public, verifiable certificates, which can speed up onboarding and compliance checks. Not all providers offer this feature.

Do I need a separate AR for the UK?

Yes, the UK requires its own representative for many regulations post-Brexit. REP27 and some others offer both EU and UK appointments under one contract and invoice, simplifying compliance for cross-border sellers.

How long must I keep compliance documents?

Declarations of conformity and related documents must be retained for at least 10 years after the last product is placed on the EU market, as required by CE marking and GPSR. Your AR may request these at any time.

Sources

  1. REP27 Europe Services SE profile — rep27.com
  2. REP27 services and pricing — rep27.com
  3. Cleo Labs EU Authorised Representative — cleolabs.co
  4. EaseCert EU Authorised Representative Service — easecert.com
  5. Conformity Point EU Authorised Representative — conformitypoint.com
  6. ProductIP Services PDF — productip.com
  7. Authoriseme.eu pricing — authoriseme.eu
  8. General Product Safety Regulation (EU) 2023/988 — en.wikipedia.org
  9. CE marking requirements — en.wikipedia.org
  10. Medical Device Regulation MDR/IVDR — reddit.com
  11. European authorised representative definition — en.wikipedia.org
  12. Machinery Regulation (EU) 2023/1230 — gdprrepresentative.com
  13. REACH Only Representative — en.wikipedia.org
  14. GDPR Article 27 requirements — en.wikipedia.org
  15. Authorized representative duties (Medical Devices) — euro-chamber.eu
  16. Non-compliance risks and costs — gdprrepresentative.com

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