Assigned EU entity
CE representation requires a written mandate and scope review. The manufacturer retains its conformity obligations; this service does not issue CE certification.
EU market access · CE
CE Authorized Representative
A dedicated workspace for CE products: regulatory scope, evidence, written mandate and authority follow-up.
Scope and mandate
1Product family
2Applicable legislation, versions and transitions
3Verified evidence
4CE representation requires a written mandate and scope review. The manufacturer retains its conformity obligations; this service does not issue CE certification.
5Incidents and authorities
Verified evidence
Specialist regimes require a dedicated assessment before acceptance. The evidence checklist is a service review policy, assessed for the product by staff.
Incidents and authorities
A dedicated workspace for CE products: regulatory scope, evidence, written mandate and authority follow-up.
CE scope
When is a CE Authorized Representative relevant?
The answer depends on sector legislation, operator roles and the exact product. The mandate never replaces the manufacturer’s conformity assessment.
A non-EU manufacturer seeking to delegate tasks permitted by the applicable legislation
A product intended for the EU market and covered by legislation requiring or permitting CE marking
A need for an EU entity to retain evidence, answer authorities and follow corrective action
A controlled path from application to active mandate
Qualification
Identify the product, intended use, markets and potentially applicable legislation.
Evidence review
Review the EU declaration, technical file, tests, labelling and notified body where required.
Scope and quote
Define models, delegated tasks, term, retention, limits and custom pricing.
Signature and activation
Assign the entity, obtain both signatures and activate after payment confirmation.
What the service organises
- Written mandate by accepted product, family or SKU
- EU entity and contact details usable only within the active scope
- Document vault with review status and expiry dates
- Authority requests, incidents and corrective-action follow-up
- History and audit-file export
What the service does not replace
- Manufacturer design, production and risk assessment
- Laboratory testing or notified-body assessment
- A certificate or official permission to use CE marking
- Customs importer, distributor or fiscal representative roles
Documents usually requested
EU declaration of conformity
Technical file and risk assessment
Test reports and applied standards
Labelling, marking, instructions and warnings
Notified-body certificates where required
Exact list of covered models and markets
Custom plan
A CE offer tailored to your products
Each CE scope depends on the products, applicable legislation, document volume and required service level.
Custom quote
Your proposal specifies the product count, covered regulations, mandate term, deadlines and payment conditions.
Request a quoteBy applying for representation, you accept the CE Authorized Representative service terms. The signed mandate defines the final scope.
CE representation questions
Does a CE Authorized Representative issue a CE certificate?
No. The manufacturer establishes conformity and the EU declaration. A notified body is involved only where the legislation and procedure require it.
Must every product bear CE marking?
No. CE marking applies only to products covered by EU legislation that requires it. It must not be affixed to other products.
Does the mandate automatically cover my entire catalogue?
No. Only products, models, legislation and tasks listed in the signed mandate and accepted after review are covered.
When does the mandate become active?
After file acceptance, EU entity assignment, both signatures and active payment of the custom plan.
Does the manufacturer remain responsible?
Yes. It remains responsible for design, conformity, technical documentation, testing, the EU declaration and marking.
Prepare a verifiable CE scope
Describe your product, models and markets. The team confirms the legislation, expected evidence and tasks that may be included in the mandate.
Apply for CE representationCandidate legislation — subject to review
Specialist regimes require a dedicated assessment before acceptance. The evidence checklist is a service review policy, assessed for the product by staff.
Low Voltage · 2014/35/EU ↗EMC · 2014/30/EU ↗Radio Equipment · 2014/53/EU ↗RoHS · 2011/65/EU ↗Toy Safety · 2009/48/EC ↗Machinery · 2006/42/EC / (EU) 2023/1230 ↗PPE · (EU) 2016/425 ↗Other / specialist assessment ↗