RoHS
Restriction of hazardous substances in electrical products
Conformity with EU product safety requirements. Typically about 7 working days after complete documents, payment and review.
The CE mark shows that a product meets the safety, health and environmental requirements of the European Union laws that apply to it. The manufacturer is responsible for the assessment, the technical file and the Declaration of Conformity. We review your product documents and issue a certificate of conformity under ISAO.
Review the CE Marking preparation checklist
Identify activities, sites, the standard and edition, and any buyer or tender accreditation requirement.
Check the issuing body, accreditation scope, assessment arrangements and total fees in writing before payment.
Submit initial business documents and the records needed to demonstrate how your management system operates.
The applicable review or audit may require additional evidence and corrective action. Timing depends on scope and readiness.
Issuance depends on successful review, not payment alone. Check the issued scope and arrange applicable surveillance and renewal.
These establish who is applying and the proposed business scope. They are the starting point; the service-specific review or assessment can require additional operational evidence.
Udyam, incorporation certificate or shop licence.
Your business name and contact details.
A recent sales or purchase invoice.
What you do, in one or two clear lines.
Use these conformity with eu product safety requirements checks to organise your preparation. For each item, identify the responsible person, the procedure used and a recent record showing what happens in practice.
Our certificate does not replace assessment by an EU Notified Body where EU law requires one for your product category.
Use the published price alongside the agreed scope and service terms when deciding whether the offering meets your requirement.
Certification and accreditation have different roles. See ISO's guidance on choosing a certification body.
This is to certify that the management system of
YOUR BUSINESS NAMEhas been assessed against the requirements of
The sample shows the layout. Issued records include your company, certified scope, applicable standard, dates and status. Specialist schemes follow their own issuer requirements.
Verify a certificateNo. For most products the manufacturer declares conformity. The CE mark is placed by the manufacturer after completing the assessment.
No, but some do, such as certain medical devices, PPE and pressure equipment. Those products need assessment by an EU Notified Body.
Only products covered by specific EU laws, such as machinery, low voltage equipment, toys, PPE and medical devices.
Explore related standards for your business.
Restriction of hazardous substances in electrical products
EU chemical regulation compliance
Quality management system
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