EAC Compliance Assessment and Certification Support
Identify applicable regulations and required documents before arranging testing and applications, aligned with your shipment plan.
Discuss your needs →- Market
- Russia and applicable EAEU markets
- Delivery method
- Technical-document review; samples, tests and applications follow the scheme
- Timing approach
- Assess regulations and scheme before scheduling tests and filing
Who it suits and prerequisites
For manufacturers, brands, traders and import partners preparing to supply Russia or other EAEU markets and needing a conformity route.
Provide sufficient information on use, models, key parameters and manufacturer, together with applicant and batch/serial plans. Incomplete information must be supplemented before a conclusion.
Scope and deliverables
| Module | What we do | What you receive |
|---|---|---|
| Initial assessment | Identify product, regulations and conformity route | Agreed regulations, document type and scheme |
| Testing and application | Coordinate suitable bodies, files, samples and tests | Technical checklist, test progress and application records |
| Document handover | Check scope, validity and registration information | Applicable result documents, checks and maintenance guidance |
Optional: specialist technical files, extra testing, production-assessment coordination and ongoing support. Sample shipping/customs and national-specific matters have separately agreed scope.
Documents and your participation
| Document | Requirements and purpose | When needed |
|---|---|---|
| Product identification | Names, models, photos, manual, use and target users | Initial assessment |
| Technical/manufacturing information | Materials, structure, key parameters, wireless functions, manufacturer and production address | Scheme and testing preparation |
| Reports and model relationships | Genuine existing reports and model differences for evidence assessment | Scheme review |
| Applicant and supply plans | Applicant, batch/serial plans and proposed customs code; sample details follow assessment | Before application and sample preparation |
Process and responsibilities
| Stage | Our responsibility | Your participation | Completion milestone |
|---|---|---|---|
| Assess regulations | Review product, regulations and route | Supply complete technical and use information | Confirmed regulations and scheme |
| Prepare | List technical files, samples and body requirements | Confirm applicant and prepare files/samples | Confirmed files and testing arrangements |
| Test and assess | Follow testing, assessment and issues | Supply clarifications and agreed corrections | Test and assessment results |
| File and hand over | Coordinate application/registration and checks | Check entities, models and documents | Results and maintenance checklist |
Timing and progress updates
- Product-specific timing: once documents, regulations, tests and scheme are clear, plan samples, testing, assessment and registration separately.
- Define the starting point: laboratory testing starts after compliant receipt of samples and fulfilment of test conditions, not at enquiry or sample dispatch.
- Dependencies include transport/customs, laboratory availability, corrections, production assessment and registration; one timeline cannot apply to all goods.
- Updates at scheme approval, sample receipt, test issues, results and registration; additional tests or corrections require an updated plan.
Important conditions and boundaries
- A certificate, declaration or other document depends on applicable regulations and scheme; both are not required for every product.
- Sample quantities, validity, production assessment and surveillance depend on the scheme. Check the body’s credentials and scope.
- Exemption statements do not replace applicable obligations. National requirements, import and marking need separate review. Test or approval outcomes cannot be guaranteed.
Aftercare and ongoing support
Handover identifies scope, validity and applicable surveillance, renewal or information-update obligations.
Review model, construction, manufacturer, production-address or applicant changes before relying on existing documents; agree ongoing support separately.
Evidence and delivery checks
Check applicant, manufacturer, models, regulations, validity and register status through the EAEU certificate and declaration register. Decisions need product-specific evidence, regulations and a scheme, rather than a category label alone.
Frequently asked questions
Is the product name sufficient?
Usually not. Use, parameters, intended users, construction and model differences can affect the requirements.
Are samples always needed?
This depends on regulations, evidence and scheme. If needed, quantity, specifications and transport requirements are listed.
Can one document cover every model?
Model relationships, differences and the scheme must be assessed. Coverage follows the final confirmed document scope.
Discuss your needs
Send a request and a business liaison will contact you within one working day to arrange this service.