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Dietary Supplement Registration

For the production and distribution of dietary supplements in the territory of the Russian Federation, these products should be registered by the Federal Service for Supervision of Consumer Rights Protection and Human Well-Being (Rospotrebnadzor).

We will execute the registration, re-registration and introduction of amendments into the Registration Documentation of Russian and foreign dietary supplements.

We have over 10 years of experience in state registration and certification of Russian and foreign dietary supplements in the territory of the Russian Federation.

The registration services will be supplied by one of the best experts in this field, possessing the highest degree of competence.

We will carry out the work for a reasonable remuneration, in the optimum time; we will also provide a flexible system of payments.  


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Our company provides the following services for certification of the dietary supplements:


  •  Assistance in preparing a registration papers at all stages of the product registration process;
  •  Organization and support during the testing of products;
  •  Organization and support in obtaining an expert opinion; 
  •  Organization and support in obtaining the Rospotrebnadzor certificate;
  •  Receipt of the Declaration of Conformity.     


When obtaining the expert opinion, our specialists organize and accompany the dietary supplement testing on the basis of specialized accredited institutions. 


Stages of Dietary Supplement Registration:


  •  Checking the composition for compliance with the current legislation requirements
  •  Preparation of the papers and product samples for testing
  •  Laboratory examination of the product samples
  •  Registration of the test reports and expert opinion
  •  Submission of the papers and expert opinion to Rospotrebnadzor
  •  Obtaining the certificate 


Certificate Acquisition Time

The terms for obtaining the state registration certificate are about 3-4 months. 

This period includes the testing, in the case when the testing laboratory does not have any additional questions to the product.

Actually the terms are the following: 

  • Testing – 1.5-2.5 months;
  • Obtaining the certificate – 15 working days. 
  • Voluntary certification on the effectiveness of the declared properties – 1.5-3 months. 


Benefits of Working With Us:

  • Guaranteed registration of the dietary supplements;
  • Providing services in this area for more than 10 years. 
  • Individual approach to each customer, flexible interaction system.



General Information 



The certificate of state registration (CSR) of the dietary supplements is issued by the Federal Service for Supervision of Consumer Rights Protection and Human Well-Being of the Russian Federation (Rospotrebnadzor).

The registration certificate is valid indefinitely.

The state duty for the CSR is 5,000 rubles ($79). 


Documents required for the Dietary Supplements



Goods Manufactured Inside the Eurasian Customs Union (EACU):

  1. an application;
  2. copies of documents in accordance with which the supplement is produced (standards, technical conditions, regulations, technological instructions, specifications, recipes, composition specifications), certified by the manufacturer;
  3. a written notification from the manufacturer that the supplement meets the requirements of the documents in accordance with which it is made;
  4. a manufacturer's document on the use (operation) of the supplement, (instruction, manual, datasheet, recommendations) or its copy certified by the applicant (if any);
  5. copies of labels (packaging) or their layouts for applied goods, certified by the applicant;
  6. copies of documents on the specific activity of the supplement (for products containing unknown components, unofficial recipes), certified by the applicant;
  7. a sampling certificate;
  8. a manufacturer's declarations on the presence of genetically modified (transgenic) organisms, nanomaterials, hormones, pesticides;
  9. testing reports (hygienic certificates), scientific reports, expert opinions;


The applicant is responsible for the accuracy of the documents provided for issuing a document confirming the safety of products (goods).

Goods Manufactured Outside the Eurasian Customs Union (EACU):

  1. an application;
  2. copies of documents in accordance with which the supplement is produced (standards, technical conditions, regulations, technological instructions, specifications, recipes, composition specifications), certified in accordance with the legislation of the Party where state registration is conducted;
  3. a manufacturer's declarations on the presence of genetically modified organisms, nanomaterials, hormones, pesticides;
  4. a manufacturer's document on the use (operation) of the supplement, (instruction, manual, datasheet, recommendations) or its copy certified by the applicant (if any);
  5. a written notification from the manufacturer that the supplement meets the requirements of the documents in accordance with which it is made;
  6. a copy of the manufacturer’s document certifying the safety and quality of the samples examined, certified in accordance with the legislation of the Party where state registration is conducted;
  7. copies of labels (packaging) certified by the applicant;
  8. originals or copies of documents on the specific activity of dietary supplements (for products containing unknown components, unofficial formulations), certified in accordance with the legislation of the Party where the state registration is conducted;
  9. a copy of the document from the authorized health authorities (other state authorized bodies) of the country of origin, confirming safety and allowing free circulation of the product in the territory of the state of the manufacturer, certified in accordance with the legislation of the Party where state registration is conducted, or the manufacturer's notification of no need for such a document;
  10. testing reports (hygienic certificates), scientific reports, expert opinions;
  11. copies of documents confirming the importation of samples of the supplement to the customs territory of the EACU, certified in accordance with the legislation of the Party where the state registration is conducted.


The manufacturer's documents shall be translated into foreign languages in accordance with the legislation of the Party where the state registration is conducted.

The applicant is responsible for the accuracy of the documents provided for issuing a document confirming the safety of products (goods).

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