REP27REP27 Contact Appoint REP27
Buyer's guide

Process for Appointing an EU Authorised Representative: Complete Guide

Short answer: To appoint an authorised representative in the EU, a non-EU business must select a provider established in the Union, sign a written mandate specifying the tasks, and ensure the representative’s details appear in compliance documents. The process varies by regulation but always requires a verifiable EU-based contact. See below for step-by-step guidance, costs, and provider comparisons.

Updated · 11 sources checked

Providers compared

ProviderEstablished inPublished priceWhat the price includesBest for
REP27Czech Republicfrom €290/year (GDPR), €190/year (GPSR), €1,490/year (AI Act)Mandate signed by Europe Services SE, verifiable certificate, one contract/invoice, human review, public verification pageNon-EU businesses needing rapid, verifiable appointments for GDPR, product, AI, or multiple EU obligations
Clever RepresentativesourceSweden€19/month (annual) or €24/month (monthly)Up to 5 products, certificates, listing on cemarked.eu, email support, 2h authority assistanceSmall non-EU manufacturers needing basic product AR for up to 5 products
AuraDPPsourceSlovakiaFrom €99/monthEU AR, EC REP, GPSR Responsible Person, covers multiple product regulations, support for packaging, WEEE, cosmeticsNon-EU manufacturers with diverse product lines and multi-regulation needs
EU ShieldsourceNot specified€490/yearGDPR Article 27 EU Representative, covers all 27 EU states, 30-day money-back guaranteeNon-EU businesses needing GDPR Article 27 representation
MyCEChecksourceNot specified€349/yearEU Authorised Representative, EU address, certificate, liaison with authorities, 2h supportNon-EU manufacturers needing AR and basic compliance support
MedexsourceNot specifiedOn requestEU AR for medical devices/IVDs, EUDAMED registration, document holding, authority liaisonNon-EU medical device/IVD manufacturers

Prices as published on each provider's website on 27 October 2026, excluding VAT unless stated. Each row links to its source.

What the Law Requires: Articles and Obligations

Several EU regulations require non-EU companies to appoint an authorised representative (AR) or legal representative before accessing the EU market. The specific obligation and legal article depend on your business activity:

The AR must be a natural or legal person established in the EU, appointed via a written mandate. Their contact details must be included in privacy notices, product labels, technical files, or compliance statements as required by the relevant regulation. The AR acts as a contact point for EU authorities and, in some cases, for consumers or data subjects. The non-EU business remains legally responsible for compliance, but the AR may be required to cooperate with authorities, hold technical documentation, or submit filings on the business’s behalf.

How to Choose an Authorised Representative: What Matters Most

Choosing the right AR is critical for compliance, business continuity, and cost control. Here’s what to consider:

ProviderIncludedNot includedExtra fees
REP27Mandate, certificate, public verification, human reviewLegal advice, product testingOn request
Clever RepresentativeUp to 5 products, certificate, supportMore than 5 productsOn request
AuraDPPMulti-regulation AR, supportOn requestOn request
EU ShieldGDPR AR, money-backOther regulationsOn request
MyCECheckAR, certificate, 2h supportExtra supportOn request
MedexMedical device AR, EUDAMEDOther productsOn request

Always request a sample certificate or verification link before committing, and confirm what is included in writing.

What the Price Really Includes (and Hidden Costs)

Published prices for EU authorised representative services can be misleading if you do not check what is actually included. Here’s a breakdown based on available data:

Common hidden costs to watch for:

Always request a detailed quote and a sample contract before signing. Ask specifically about any recurring or per-request fees, and clarify whether certificates and public verification are included in the base price.

How Appointment Works: Step by Step

The process of appointing an EU authorised representative is structured but can vary in detail between providers. Here’s a typical step-by-step process, with examples from REP27 and other providers:

  1. Identify Your Regulatory Obligations: Determine which EU regulations apply to your business (GDPR, GPSR, AI Act, Data Act, Medical Devices, etc.). Use provider checklists or free online tools to confirm your needs.
  2. Choose a Qualified Provider: Select a provider established in the EU and suited to your obligations. For example, REP27 covers multiple regulations with one contract, while others may focus on a single area.
  3. Submit Your Company File: Provide details such as your company name, registration, address, product or service information, and target markets. REP27 requires this before any appointment is signed.
  4. Human Review: A staff member reviews your file for completeness and compliance. REP27 performs this within 24 working hours. If information is missing, you will be contacted for clarification.
  5. Mandate Signature: Once your file is approved, the provider’s statutory body signs a written mandate specifying the AR’s tasks and responsibilities. For REP27, this is Europe Services SE.
  6. Receive Certificate and Instructions: You receive a signed certificate, sometimes with a QR code and verification code, and the exact wording to use in your privacy notice, product label, or technical file.
  7. Public Verification (if available): Some providers (like REP27) offer a public verification page showing your company name, the service, status, and validity dates—never your internal data.
  8. Update Compliance Documents: Add the AR’s details to your privacy notice, product labels, technical files, or online store as required by law.
  9. Ongoing Support: Use included support hours for authority queries or compliance questions. For additional needs, check if extra fees apply.

Checklist for Buyers:

  1. Confirm which EU regulations apply to your business.
  2. Gather company and product/service details.
  3. Request offers from several AR providers and compare inclusions.
  4. Ask for sample certificates and public verification links.
  5. Review contract terms, notice periods, and support conditions.
  6. Sign the mandate and update your compliance documentation.
  7. Keep the certificate and verification code accessible for audits or marketplace requests.

Risks, Fines, and What Providers Usually Do Not Say

Failure to appoint a compliant EU authorised representative can result in serious business and legal consequences. Here are the main risks and what to watch for:

What Providers Usually Do Not Say:

To avoid surprises, always request the full contract and a detailed breakdown of included services, support, and notice periods before signing.

Decision Matrix: Do You Need an EU Authorised Representative?

Not every non-EU business needs an EU AR. Use this decision matrix to check your situation:

If you are...You need...You do not need it if...
Non-EU business selling to EU consumers (B2C)GDPR AR, Product Responsible Person, possibly AI/Data Act ARYou only sell to non-EU customers and do not process EU data
Non-EU business selling via Amazon/Etsy/eBayProduct Responsible Person, sometimes GDPR ARYour products never reach EU consumers
Non-EU SaaS or cloud serviceGDPR AR, NIS2/Data Act ARNo EU users or data processed
Non-EU manufacturer of medical devicesMedical Device ARDevices not placed on EU market
Non-EU B2B supplier with no EU end usersOn requestNo direct EU market presence

For marketplaces, check their onboarding requirements: Amazon, eBay, and others often require proof of AR appointment for non-EU sellers. For SaaS and cloud, GDPR AR is required if you process or monitor EU personal data, regardless of company size.

Realistic Scenarios: What Applies and What to Do

In each scenario, the process involves: identifying obligations, choosing a provider, submitting required information, signing the mandate, receiving the certificate, and updating compliance documents. Always keep your AR’s details and certificate accessible for audits, customs, or marketplace requests.

When you do not need this

Frequently asked questions

What is an EU authorised representative?

An EU authorised representative (AR) is a person or company established in the EU who acts on behalf of a non-EU business for regulatory compliance, such as GDPR, product safety, or AI Act obligations. The AR is appointed by written mandate and appears in compliance documents and labels.

Who needs to appoint an EU authorised representative?

Non-EU businesses that sell products, handle personal data of EU residents, offer AI or connected services, or place regulated goods (e.g., medical devices, cosmetics) on the EU market must appoint an AR. The requirement depends on the specific EU regulation.

How long does it take to appoint an EU AR?

With REP27, the process usually takes 24 working hours after submitting a complete file. Other providers’ timelines may vary and depend on their internal review process and required documentation.

What documents are needed to appoint an AR?

Typically, you need to provide your company details, product or service information, and compliance needs. Some providers may request technical files, product lists, or proof of business registration.

Does the AR take legal responsibility for compliance?

The AR acts as a contact point and may perform certain regulatory tasks, but the non-EU business remains legally responsible for compliance under most EU regulations.

Can I change my AR later?

Yes, but check your contract for notice periods or transfer fees. You must update all compliance documents and notify authorities or marketplaces of the change.

Is one AR enough for all EU obligations?

Not always. Some providers (like REP27) cover multiple regulations, but others may only cover one (e.g., GDPR or product safety). Review your obligations before choosing.

What happens if I do not appoint an AR?

You risk fines, blocked shipments, removal from marketplaces, or being unable to sell to EU customers. Authorities may also refuse to process your compliance filings.

Do I need an AR for B2B sales?

It depends. For some regulations (e.g., medical devices, product safety), the requirement applies regardless of B2B or B2C. For GDPR, if you process EU personal data, you need an AR.

Are there extra costs for certificates or support?

Some providers include certificates and limited support in the price; others charge extra for certificates, public verification, or additional support hours. Always confirm before signing.

How do I prove my AR appointment to authorities or marketplaces?

You receive a signed certificate or letter, often with a verification code or QR link. This must be shown to authorities, marketplaces, or included in your compliance documents.

Can a law firm be my AR?

Yes, but the AR must be a person or company established in the EU. Some providers are companies, not law firms, but are fully compliant if established and verifiable in the EU.

Sources

  1. REP27 Europe Services SE (official) — rep27.com
  2. Clever Representative Pricing — cleverrepresentative.eu
  3. AuraDPP EU AR Service — auradpp.com
  4. EU Shield GDPR Representative — eushield.eu
  5. MyCECheck EU Representative — mycecheck.com
  6. Medex EU Authorized Representative — medexeurep.com
  7. GDPR Article 27(3) — eushield.eu
  8. AI Act Article 54 — gdprrepresentative.com
  9. Cyber Resilience Act Article 18 — cra.docs.bauer-group.com
  10. Data Act Article 37 — gdprrepresentative.com
  11. Medical Devices Regulation Article 11 — casrai.org

Related guides

REP27See exactly what REP27 includes →