International Certification Center LLC is an accredited product certification body. A document we issue is valid across the entire Union — Armenia, Belarus, Kazakhstan, Kyrgyzstan and Russia — with no further confirmation needed in any individual country.
We work side by side with our own testing laboratory, the International Research Center. The applicant gets the full cycle in one place: sampling → laboratory testing → production audit → issue of the permitting document → entry in the register.
Absence of the document, or circulation of products on the basis of inaccurate information, entails administrative liability, withdrawal of the product from circulation and a ban on its sale.
A document certifying that the product complies with the requirements of a technical regulation. It is issued by an independent third party — an accredited certification body.
A document by which the applicant itself declares that the product complies with the requirements of the regulation. It is adopted by the applicant and registered in the unified register.
Vehicle type approval and chassis type approval — a document certifying that a vehicle type or chassis type complies with the requirements of TR CU 018/2011.
A document confirming that a product is safe against the sanitary-epidemiological and hygienic requirements. Issued indefinitely.
Other conformity assessment documents provided for by the legislation and by the acts of the Union — depending on the type of product, the market and the client's requirements.
Over 500 product positions. A single item often falls under two to four regulations at once — we run them as one file.
Confirming conformity is the certification body's own responsibility. It takes the samples itself, sends them to an accredited laboratory, inspects the production site where this is required, and decides whether the document is to be issued.
Validity is set by the technical regulation: for serially produced goods, as a rule, up to 5 years; for a batch or a single item no term is set. The applicant may be the manufacturer (including a foreign one, where it has an authorised representative in the Union), the seller or the supplier.
A declaration is adopted by the applicant under its own responsibility. A declaration and a certificate have equal legal force — both give the right to place the product on the market and to apply the EAC mark. The difference is the procedure and who adopts the document.
The applicant bears responsibility for the accuracy of the information in the declaration. That is exactly why the evidence base has to rest on reports from an accredited laboratory rather than on paperwork put together for form's sake.
The SGR confirms product safety against the unified sanitary-epidemiological and hygienic requirements of the EAEU. It is issued indefinitely, obtained before production starts or before the product is imported, and is valid across the Union. It is not an alternative to a declaration or certificate but an addition: many product types require both.
Biologically active food supplements are the most demanding object of state registration. We have developed and apply an internal guide to the sanitary-epidemiological and hygienic assessment of supplements, harmonised with the acts of the Union.
Without a type approval, new vehicles cannot be placed on the market or registered. Our scope under TR CU 018/2011 covers 99 product groups, the largest position in the scope of accreditation: from engines and braking systems to lighting, seat belts and child restraint devices.
Validity is limited by the expiry date of the requirements of the corresponding environmental class. A type approval covers vehicles placed on the market during its period of validity.
Vehicle testing is carried out by the Automotive Vehicle Research Centre →We establish which technical regulations cover the product, which form and scheme of assessment apply, and whether state registration is needed. The consultation is free.
Determination of the EAEU commodity code, the type and purpose of the product, the age group for children's goods, the composition and formulation.
The application, the list of characteristics and the test programme, agreement on deadlines and price.
Under certification schemes, samples are taken by the certification body with a sampling act drawn up.
Carried out in our own accredited laboratory, with test reports issued.
For schemes 1c, 5c and 7c — or analysis of the management system certificate for schemes 2c, 6c, 8c and 6d.
Certificate of conformity, registration of the declaration, type approval, or support of state registration.
The document is entered in the register and available for public verification.
Advice on applying the EAC mark and on labelling requirements, including those of TR CU 022/2011.
Throughout the validity of the certificate — periodic testing of samples and production audits.
The exact list is determined by the technical regulation and the chosen scheme — we draw it up individually at the consultation stage.
A certificate is issued by an independent accredited certification body, which also takes the samples and answers for the decision. A declaration is adopted by the applicant under its own responsibility and registered in the register. Both documents have equal legal force — both give the right to place the product on the market and to apply the EAC mark.
No. The form of assessment is fixed by the technical regulation for each type of product. Toys are subject to certification only; perfumery and cosmetics to declaration only. For children's goods, light industry products and personal protective equipment the form depends on the type of item, the layer it belongs to and the age group.
Not always. An electric toy falls under TR CU 008/2011, TR CU 020/2011 and TR EAEU 037/2016. Packaged mineral water falls under TR CU 021/2011, TR EAEU 044/2017 and TR CU 022/2011, and medicinal mineral water additionally requires state registration.
Yes. A document issued by an accredited body of an EAEU member state and entered in the unified register is valid across the Union without further confirmation.
For specialised food products — infant nutrition, supplements, sports and dietary nutrition, medicinal mineral waters — and for products in section II of Decision No. 299, state registration is mandatory in addition to the declaration.
Indefinitely — until the composition, the product name or the manufacturer changes.
We inform the applicant of the non-conformities found and state which characteristics failed. The applicant may rework the product and submit it again. A document cannot be issued on negative test results.