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European Union · Global Market Access

Entering the EU Market: Vehicle Type Approval (E-Mark)

Vehicle and component type approval; mandatory for road registration.

Market
European Union
Site
European
Mark
E-Mark

01What is it?

The E-Mark is the mark showing the type approval of vehicles and of vehicle systems, components and separate technical units. An E within a circle shows approval under the UNECE agreement; an e within a rectangle shows EU type approval.

02Why Does This Scheme Exist?

Conformity for vehicles and vehicle components works through an entirely separate legal route from other product legislation, and the reason is historical: the vehicle type approval system was established long before the EU's product legislation, within the framework of an agreement under the United Nations, and it still draws on that framework today.

The distinguishing logic of this arrangement is TYPE APPROVAL. Instead of a declaration per product, a vehicle or component TYPE is approved by an authority; the conformity of series production to that type is then maintained through conformity of production audits. That is, approval is obtained once and conformity is monitored continuously.

The second distinguishing feature is MUTUAL RECOGNITION: an approval granted by the authority of one country party to the agreement is accepted in the other contracting countries. The circle and number within the mark show the country that granted the approval and the approval number. This provides access to a wide geography with a single approval and is the arrangement's greatest practical advantage.

Approval subjects are numbered as regulations and each addresses a single technical subject: lighting, braking, glazing, seats, seat belts, noise, electromagnetic compatibility, power train components in electric vehicles and so on. A vehicle must obtain approval separately under every regulation applying to it.

The spread of electric vehicles added new subjects to this arrangement: high voltage safety, battery safety and the charging interface each acquired their own regulation. Cyber security and software update management systems brought a new layer that makes not the product but THE MANUFACTURER'S SYSTEM a condition of type approval.

03Whose Obligation?

The obligation lies with the manufacturer. Approval is granted by the type approval authority; the technical assessment is carried out by designated technical services. In addition to the approval, the Conformity of Production (CoP) obligation is continuous.

04Required Documents

  • The UNECE regulation or EU type approval legislation applied
  • Technical service test reports
  • The information document
  • Conformity of production (CoP) arrangements
  • The type approval certificate and approval number

05Process

  1. 01Scope DeterminationIt is determined which legislation and marking scope the product falls under in the target market. This step defines the entire process; getting it wrong wastes all subsequent work.
  2. 02Determining Applicable StandardsThe standards accepted by the market and any national deviations are identified. The same IEC standard may apply with different deviations in different markets.
  3. 03Establishing the Test PlanIt is assessed which part of existing test reports will be accepted; missing tests are planned. A CB Scheme report, if available, reduces retesting.
  4. 04Local Party and RegistrationIf the market requires an established representative, importer or applicant, this party is designated and the necessary registrations are made.
  5. 05Tests and Technical FileTests are conducted and the technical file is prepared. Some markets require testing to be performed within their own country.
  6. 06Certification or DeclarationDepending on the market's regime, a manufacturer's declaration is drawn up or a certificate is obtained from the authorised body; a factory audit is carried out if required.
  7. 07Marking and LabellingThe mark and label are applied according to the market's format and language rules. The language requirement is checked at customs in most markets.
  8. 08Shipment and CustomsIf a pre-shipment document is required, it is obtained; the document set to be presented at customs is completed.

06Points to Watch

  • Without type approval, registration and sale are not possible
  • The CoP obligation is continuous and is audited periodically
  • Changes to the type must be notified and the approval extended
  • Türkiye's approval number is 37

07Neighbouring Schemes and the Difference

  1. 01E-Mark and CEVehicles and vehicle components are as a rule outside the scope of CE; the type approval arrangement is a separate legal route. Declaring both together for the same product is contrary to the structure.
  2. 02Component approval and vehicle approvalUsing an approved component does not secure the vehicle's approval; the vehicle obtains approval separately under its own regulations. The reverse is also true: vehicle approval does not legitimise selling the component separately.
  3. 03Type approval and after-sales partsCertain items among spare parts and equipment are subject to their own approval regulation; placing an unapproved part on the market is prohibited for some items.
  4. 04Automotive EMC and general EMCFor vehicles and their components, electromagnetic compatibility is assessed under its own type approval regulation rather than the general EMC directive; the test arrangements and limits differ.

08Scheme Detail

This page describes entry into the European Union market. The scheme itself — its scope, process, validity period and required documents — is covered in detail on the certification page.

Vehicle Homologation (E-Mark) Certification

09Other Marks in the European Union Market

10Frequently Asked Questions

This section's content is being prepared. The roadmap specific to your product and target market at the quote stage in writing.

The certification timeline varies with the product, the required test workload, sample shipping time and the authority's workload; for this reason, no duration in days or weeks is given on these pages. The main factors determining the timeline are: whether testing must be performed in the target country, whether a factory audit is required, the time to appoint a local representative, and the current maturity of the technical file. A realistic timeline for your product is provided in writing at the quote stage.

Market access regimes change frequently: scope lists are updated, transition periods are extended, new requirements are added. These pages describe the structure of the regime and who bears the obligation; the applicable scope and dates for your product are confirmed from the current legislative text at the quote stage.

European Union · E-Mark roadmap for

Tell us about your product; we'll share the required steps, documents and timeline in writing.

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