Loading

European Union · Global Market Access

Entering the EU Market: Electromagnetic Compatibility (EMC)

Electromagnetic Compatibility Directive — emission and immunity requirements.

Market
European Union
Site
European
Mark
EMC

01What is it?

The EMC Directive imposes a two-way requirement: the equipment must not radiate unacceptable interference into its surroundings and must itself be able to operate as expected under interference.

02Why Does This Scheme Exist?

The problem that gave rise to electromagnetic compatibility legislation became clear in the 1980s: as electronic devices multiplied they began to disturb one another's operation. The noise produced by a power supply shifted the reading of the measuring instrument beside it; a motor drive drowned out a radio receiver. The problem was not a product's own safety but the sharing of the ENVIRONMENT.

The legislation therefore establishes a two-way requirement, and grasping this determines the whole process. On one side, EMISSION: the product shall not radiate electromagnetic energy at a level that disturbs the devices around it. On the other, IMMUNITY: the product shall maintain its function in the electromagnetic environment that can reasonably be expected. A product that meets the first condition but not the second is not compliant.

Scope is defined not by product type but by the capacity to generate an electromagnetic phenomenon or to be affected by one. The legislation therefore covers a very wide range of products, and products that "generate no electromagnetic phenomenon", such as passive components, fall outside the scope.

Under this legislation too a notified body is not mandatory; the manufacturer makes its own declaration. Obtaining the opinion of a conformity assessment body is possible but optional. Again the technical file is the only line of defence.

Environment classification is the most frequently overlooked aspect of the legislation: the standards define different emission limits and different immunity levels for residential and industrial environments. A product declared for an industrial environment cannot be sold for residential use, and this distinction must be written in the user manual.

03Whose Obligation?

Where harmonised standards are applied in full, the manufacturer makes its own declaration. Where a standard is not applied, or only partly applied, the route in which the opinion of a notified body is obtained is chosen.

04Required Documents

  • Product block diagram, cabling and earthing arrangement
  • Emission and immunity test reports
  • The list of harmonised standards applied
  • The operating mode during testing and the definition of the performance criterion
  • The EU Declaration of Conformity

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

  • Radio equipment is outside the scope of EMC; its EMC requirements are addressed within RED
  • In an immunity test the product need not be entirely unaffected; acceptable behaviour is defined in advance
  • There are separate provisions for fixed installations

07Neighbouring Schemes and the Difference

  1. 01EMC and LVDThey apply together to the same product; LVD addresses user safety and EMC compatibility with the electromagnetic environment. They are two separate test programmes and two separate sets of requirements.
  2. 02EMC and REDFor a product carrying a radio interface, the EMC requirements are met within RED; no separate EMC declaration is made. RED additionally requires the efficient use of the radio spectrum.
  3. 03EMC and automotive EMCVehicles and vehicle components are subject to their own EMC requirements within the vehicle type approval framework rather than the general EMC directive; the test arrangements and limits differ.
  4. 04EMC and harmonics/flicker requirementsHarmonic current and voltage fluctuation fed into the supply network are governed by separate standards and are part of the EMC file; they must not be confused with the emission tests.

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.

Electromagnetic Compatibility Directive (EMC) and CE Marking

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 · EMC roadmap for

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

We use cookies required for the site to work. With your permission we also add an analytics cookie to understand how pages are used. Cookie Policy