Industrial Compliance
Need RoHS evidence for an electrical or electronic product going to the EU? Start with the exact product and materials in scope, the customer's requested evidence and the supplier declarations you already have. This identifies whether you need targeted laboratory testing, documentation review, or both.
Tell us the product, model variants and the buyer's wording. ConformArc will organise the initial requirement so an appropriate materials-compliance or testing specialist can confirm the evidence plan and quote the work. You do not need to upload a confidential bill of materials to start the conversation.
Common requests: a distributor asks for a RoHS declaration; a component declaration is missing or inconsistent; a new material or supplier creates an evidence gap; or a buyer asks for a specific test report. The sample selection and test method should follow the product and material question, rather than a default test package.
A distributor asks for a RoHS declaration; a component declaration is missing or inconsistent; a new material or supplier creates an evidence gap; or a buyer asks for a specific test report. The sample selection and test method should follow the product and material question, rather than a default test package.
A specialist may start by checking product scope and any relevant exemption, then review the bill of materials, component declarations and existing reports. Testing can be used where evidence is absent, inconsistent or higher risk. The sample, homogeneous material, test method and report use must be agreed by the laboratory; do not assume that testing one convenient component covers the whole product. The required documentation and EU declaration responsibilities remain with the relevant economic operator under the applicable rules.
This page addresses EU RoHS. A customer request for REACH, WEEE or another substance regime should be stated separately. If the same electronic product also needs electromagnetic evidence, see industrial EMC testing. For a device also heading to the US, see FCC equipment authorization.
Provide product type and use, target market, model variants, bill of materials or a high-level component list, existing supplier declarations/reports, the buyer’s required format, and target date. A high-level description is enough for the first contact; share confidential BOMs with an agreed provider through an appropriate channel after scope and permission are settled.
Do not assume one. Ask the buyer what evidence it requires and have the specialist review the actual legal/product scope.
Not by default. The evidence must address applicable restricted substances in relevant materials; sample selection and documentation matter.
No. Include both in the enquiry if your customer asks for both so the provider can scope them separately.
No. A laboratory or documentation specialist confirms that work within its own agreed scope.
Requirements can change. Confirm the current route and applicable edition for the specific product before starting the project.
What is the product and EU/customer requirement? Do you need a test report, documentation review or help determining the evidence? Tell us the product, target market, current stage and customer wording. You can start without uploading confidential documents.
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