Regulatory framework · Finished products
CE marking: technical file and supplier evidence
Centralise DoC, applicable standards and component evidence before affixing the CE mark.
Framework highlights
- EU declaration of conformity
- Harmonised standards identified
- Component / sub-assembly evidence
In Suplylot
Questionnaires, grids and campaigns for CE marking
Ready-to-use templates in the buyer portal: supplier collection, automatic follow-ups and compliance tracking by reference.
- "CE marking / DoC collection" supplier questionnaire
- CE marking customer product assessment grid
- DoC and technical evidence campaigns
- Link with RoHS, GPSR and other applicable directives
Regulatory framework
CE marking attests that the product meets applicable EU directives and regulations (LVD, EMC, machinery, toys, medical devices, etc.). It relies on an EU declaration of conformity and a technical file.
Procurement must obtain DoCs and evidence on components and sub-assemblies to build an auditable finished-product file.
What the buyer must require
Evidence needs to be verifiable, dated and tied to a specific reference. A generic statement isn't enough.
- EU declaration of conformity (DoC) per reference.
- List of applied directives / regulations and harmonised standards.
- Technical evidence for critical supplied components.
- Identification of the manufacturer / authorised representative responsible for marking.
Manage compliance over time
Suplylot aggregates DoCs and CE marking evidence at product and supplier level, and cross-checks with RoHS, GPSR or MDR depending on the finished-product scope.
- Map applicable directives by range.
- Require component DoCs at qualification.
- Alert on expired DoCs or obsolete standards.
Useful sources
Manage CE marking across your supplier panel
Questionnaires, document files and collection campaigns, from the material catalog to compliance tracking.
Already a client? Buyer portal · Supplier portal