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Food Supplement Registration in Kazakhstan

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Food Supplement Registration in Kazakhstan

Regulatory Authority

The Ministry of Healthcare of the Republic of Kazakhstan

Regulatory Website

https://www.gov.kz/

Registration Timeline

5-7  Months

License Validity

Permanant

Like any product, dietary supplements must be registered with the state. The Committee for the Protection of Public Health of the Ministry of Health of the Republic of Kazakhstan is responsible for the state registration and re-registration of nutritional supplements in our country.

The following food items are considered special purpose:

  • Nutritional supplements that are biologically active;
  • Sports nutrition;
  • Food items and nutrients meant for expectant and nursing mothers;
  • Food for infants;
  • Food items intended for nutritional therapy and prevention.
  •  

Documents for Food Supplement Registration in Kazakhstan

  • Copies of documents certified by a producer based on which the products are manufactured.
  • Standard or organizational standard, technical condition, manufacturing specification formulation.
  • Written notification from a manufacturer (producer) certifying that the manufactured products comply with the requirements of documents based on which the products are manufactured. The following is accepted as a notification: copies of quality certificate, safety (quality) certificate, quality certificates certified by a manufacturer (producer) or a letter from a manufacturer (one of the listed documents is to be provided).
  • Document from a manufacturer (producer) on application (operation, use) of products (instruction, guidance, recommendation) (one of the listed documents) or a copy certified by an applicant.
  • Copies of labels (packages) and their models certified by an applicant.
  • Original copy of sampling certificate issued by laboratories (centers) accredited (certified) in national accreditation (certification) systems and included in the Unified Register of Certification Bodies and Test Laboratories (Centers) of the EEU.
  • Original copy of studies (tests) issued by laboratories (centers) accredited (certified) in national accreditation (certification) systems and included in the Unified Register of Certification Bodies and Test Laboratories (Centers) of the EEU.
  • Original copy of a scientific report issued by a profile scientific institute or profile scientific center executing activities in the field.
  • Original copy of expert evaluation issued by a profile scientific institute or profile scientific center executing activities in the field.
  • In cases when a manufacturer uses nanomaterials in perfume and cosmetics, it is necessary to provide information about the nanomaterial, including its chemical name, particle size, and physical and chemical properties
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