Conformity Point
CE marking compliance services for consumer products

CE Marking Compliance Services

For consumer products

Choose the level of CE marking support you need: diagnostic review, technical file preparation or full compliance process management for consumer products sold in Europe.

Three levels of CE marking support based on your available documentation and the help you need. From €119 per product.

24h responseClear timelinesNo last-minute surprises
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CE marking consulting services — Plans and pricing

Choose the level of CE marking support based on your available documentation and the help you need.

Diagnostic Plan

from€119/ productPrices exclude VAT.

Technical assessment and action plan

What's included:

  • Product technical assessment
  • Definition of applicable regulations
  • Review of available documentation
  • Conclusion and next steps
  • Second review included

Ideal for:

  • Knowing exactly what you need before investing
  • Validating whether your supplier documentation works for Europe
  • Confirming whether your product is ready to launch or needs corrections
Request Diagnostic
Most requested

Technical File Plan

from€199/ productPrices exclude VAT.

Complete technical documentation

What's included:

  • Review of available documentation
  • Update of the pending actions guide
  • Drafting of the product risk assessment
  • Preparation of the EU Declaration of Conformity
  • Preparation of the complete technical file
  • Definition of mandatory markings on product and packaging
  • Specification of mandatory warnings and instructions for the manual
  • GPSR warning recommendations for web listings

Ideal for:

  • Having a technical file ready to present to buyers or authorities
  • Selling on Amazon, retail, or EU B2B
  • Meeting GPSR and marketplace requirements
Request Technical File

Full Plan

from€599/ productPrices exclude VAT.

Full management of the compliance process

What's included:

  • Product technical assessment
  • Definition of applicable regulations
  • Review of available documentation
  • List of required tests
  • Coordination with the supplier to collect valid reports
  • Planning and management of testing with the laboratory
  • Drafting of the product risk assessment
  • Preparation of the EU Declaration of Conformity
  • Preparation of the complete technical file
  • Definition of mandatory markings on product and packaging
  • Specification of mandatory warnings and instructions for the manual
  • GPSR warning recommendations for web listings
  • Project follow-up until all documentation is available

Ideal for:

  • Complex launches or critical products
  • Full delegation of the compliance process
  • Coordination with labs and suppliers without you having to manage it
Request Full

Base rates

The service price depends on the product, applicable regulations and its risks. We confirm the scope and price before you commit. More complex products require a specific quote.

Laboratory testing, Notified Body fees and other third-party costs are quoted separately.

Illustrative examples

Base rate
  • Board game
  • Electric blender
  • Rechargeable lamp
Quote required
  • Remote-controlled car
  • Food processor with Wi-Fi
  • Rechargeable speaker with LED

Move forward in stages

You can start with the Diagnostic Plan and upgrade to the Technical File Plan by paying the difference within 30 days of delivery of the diagnostic.

Diagnostic Plan → Technical File Plan
Paid119
Additional80
Total199 €

Not sure which one to choose?

Request a free consultation

We'll recommend the right service for your case.

Need something different?

If your situation doesn't fit any plan, contact us and we'll prepare a customized proposal.

If you also need an EU Responsible Person—common when you sell from outside the EU without an established importer—we offer it as a separate service. Authorized Representative support is available where applicable.

See Responsible Person plans
View EU Authorised Representative service

What the CE marking technical file includes

The technical file

Complete set of documentation supporting the Declaration of Conformity: technical product description, drawings and schematics, risk assessment, EU Declaration of Conformity, test reports, component certificates, instruction manual, labeling specifications, and change log. As a general rule, it must be kept for 10 years and made available to market surveillance authorities when requested.

The risk assessment

Systematic evaluation of all potential product hazards during normal use and reasonably foreseeable misuse: electrical, mechanical, chemical, and thermal hazards. It identifies severity and likelihood for each risk and documents the mitigation measures applied. It is the central document of the technical file and the first one authorities request during an inspection.

The EU Declaration of Conformity

Legal document in which the manufacturer declares under its sole responsibility that the product complies with all applicable European Directives. It must include manufacturer identification, product description, complied Directives, applied standards, and the signature of an authorized person. Without it, you cannot affix the CE marking or legally sell in Europe.

Mandatory markings on product and packaging

Visible, legible, and indelible indications that must appear on the product and its packaging: CE marking, manufacturer identification, model/type, batch or serial number, the address of the responsible economic operator established in the EU (importer, authorized representative, or fulfilment service provider), when applicable, and mandatory safety warnings depending on the product category.

Warnings and instructions in the manual

Safe-use guidance, residual hazard warnings, and mandatory maintenance instructions depending on the product category. They must be in the language of the country where you sell. A well-written manual reduces legal risk and meets consumer information obligations.

GPSR warnings for web listings

For online sales, the GPSR requires that the offer displays minimum manufacturer/operator information and relevant safety warnings and safety information. Applicable from 13 December 2024 for products within the scope of the GPSR.

Laboratory testing

Technical tests verifying that the product meets safety requirements, electromagnetic compatibility, performance, and any other aspect regulated by the applicable Directives. They are the objective evidence of compliance. Without recognized laboratory testing, the technical file will not withstand inspections or marketplace requirements.

Tell us what product you have and we'll tell you what you need

Tell us what you sell, where you are in the process, and what documentation you have. Within 24 hours, we'll tell you which CE marking consulting plan you need, how much it costs, and how long it takes.

Talk to a consultant

FAQs about our CE marking consulting services

Two products are considered the same if they keep the intended use, function, main materials, and risk profile. Color, size, cosmetic dimensions, or packaging may vary. They are considered different if the main material, critical components (battery, circuit), function, target population (adults vs. children), or electrical characteristics change. Example: LED flashlight in 3 colors = same product. Rechargeable LED flashlight vs. battery-powered = different products.

It mainly depends on laboratory testing time: 2–3 weeks for simple products and up to 6–8 weeks for complex products or those with multiple certifications. Technical documentation preparation is relatively fast once you have the test results.

Yes, if they are valid. We review what works and what doesn't. For a certificate to be valid, it must cover your exact product (same model, components, and specifications), come from a recognized lab, be based on the current version of the standard, and cover the applicable Directives. If it meets these criteria, we integrate it into the technical file. If not, we tell you what you need to complete.

Yes. EU (CE marking) and UK (UKCA marking) technical requirements are very similar, and we can prepare documentation valid for both markets. We confirm your product's up-to-date status within 24 hours.

Yes, if you are a manufacturer outside the EU and there is no established importer in the EU. In that case, to sell in the EU there must be a responsible economic operator established in the Union (for example, an importer, an authorized representative, or a fulfilment service provider), under the GPSR applicable from 13 December 2024. We offer it as a separate service, contracted together with the consulting service or separately.See Authorized Representative service

We prepare urgent unblocking documentation with what you have available so you can respond quickly. Then we complete the full technical file. In urgent cases, we can prioritize your project for an additional fee.

Yes. If you purchase an upgrade within 30 days of delivery of the diagnostic or previous stage, we deduct the total amount actually paid for earlier stages for the same product and scope from the new service’s total price. This also applies to the full-service plan and, for incident services, to the same incident and scope. At the base rates, if you have paid €119 and the next service’s total price is €199, you pay an additional €80. For individually quoted work, we confirm the total price before the upgrade and deduct the amount already paid.

It does not formally expire, but it must be updated if you change critical components, new versions of harmonized standards are published, or you modify design, packaging, or intended use. In practice, documentation older than 5 years may not be accepted by certain sales channels.

A person authorized to legally represent the manufacturer: the CEO, the technical director, or anyone with documented legal authority. The signature assumes legal responsibility for product compliance.

It is an EU-authorized entity to perform conformity assessments for high-risk products when the applicable Directive specifically requires it. For most consumer products, it is NOT mandatory. We confirm in the initial assessment whether your product requires it.

Yes. If you put your brand on the product, modify anything that affects conformity, or assume conformity responsibility, you are legally the manufacturer. You need a technical file in your name, not only the original manufacturer's.

No. It is a separate service. If you sell from outside the EU and there is no importer/economic operator established in the EU, you will need a responsible economic operator established in the EU. If you contract both, the risk assessment and the Declaration of Conformity are not duplicated—we help you set up the right combination.See Authorized Representative service

Product description (what it is, how it works, intended use), technical specifications (voltage, power, materials, dimensions), photos of the product and current labeling, and any existing documentation (certificates, test reports, manuals). We send you a detailed checklist when you request the service.

No. US standards are not valid for CE marking. You will need testing to European harmonized standards.

The final price depends on the product’s characteristics, applicable regulations, complexity and risks. We review the product and available documentation to confirm the scope and price before you commit. More complex products and work beyond the base scope require a personalised quote.

More questions? Talk to us directly.

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