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CE Marking and Product Compliance Services
CE preparation based on the actual product, intended use, applicable laws, evidence gaps and manufacturer or assessment-body tasks.
Choose a product route before ordering CE work
Use this page to select the preparation task and the relevant product guide before requesting a quotation.
Define the product and the legislation
Identify the finished product, models, intended use, supply and operating conditions, manufacturer and target market. Start with the actual law that requires CE, not a purchased certificate or a preferred standard number. A product may fall under several applicable rules; a mark is not permitted merely because the buyer requests one.
Use the service links below to investigate the actual product family. A machine, medical device, radio product and construction component do not share one approval procedure. An ISO management-system certificate does not decide the product route, and national non-EU market requirements remain a separate check.
Decide what existing reports really support
Compare each report with the sold model, component list, material, software, configuration and intended operating conditions. Record the requirement, evidence method, report boundary and unresolved difference. Select additional review or tests from that gap; there is no universal CE test package that closes every product requirement.
For example, a wireless control unit changes antenna and power supply after its earlier tests. Identify the changed configuration and relevant radio, electrical and other applicable requirements before reusing reports. The old brand name or a CE-marked module does not establish conformity of the changed finished product.
Separate the responsible parties and outputs
The manufacturer remains responsible for the actual product and the applicable declaration, technical documentation and marking. Determine whether the lawful route allows manufacturer assessment or requires a notified body. Where required, check current NANDO designation for the relevant legislation, product and procedure, rather than accepting a consultancy logo.
A test laboratory supplies results within its work scope; a notified body performs its designated task; Kayra can help with contracted scope and evidence preparation. None of these roles automatically transfers all manufacturer duties. A voluntary certificate, registration or quotation is not the required conformity decision or declaration.
Request a defined preparation service
Send product identification, intended use, markets, model differences, existing complete reports, drawings and the requested task. Distinguish route/gap review, documentation, testing coordination and required external assessment. Keep the existing internal guides for the detailed family route; this hub helps select the right work before a quotation.
Agree who provides data and samples and who decides report acceptance. A changed design or deficient report may reopen work. Preparation, laboratory and body costs and their dependencies should be separate; a fixed favourable decision, blanket market permission or guaranteed CE date cannot be promised.
Related internal guides
Choose a product route before ordering CE work
What Are Importer and Distributor Responsibilities for CE Marking?
Understand CE marking duties for importers and distributors: document checks, traceability, labels, instructions, storage and non-compliance action.
Read the article →Get a scope-based assessment
Share the subject, organisation or product, target market, current evidence and target date. The team can then separate consultancy, official fees, independent evaluation and realistic timing.