State registration of food supplements in Kazakhstan

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State registration of food supplements in Kazakhstan

The main objective of the registration is the confirmation of quality and safety of food supplements intended for sale

During the registration, experts review all documentation and assess the compliance of a new product as per the requirements of EEU technical regulation. After successful completion of the procedure, the biosupplement is added into the register of food supplements that have passed state registration

State registration and reregistration of food supplements is implemented by the Committee of the Ministry of Health of the RK

You will have a lot of work, the nuances of which are unknown to you: 

The procedure may take a long time

You may not know the details of the regulatory environment

You may not know the nuances of communication in regulatory bodies or in the country

We will undertake all the routine work.

You save time and therefore money

We have a team of professionals in different areas of regulatory affairs

We select individual solutions for each project

We guarantee confidentiality

We guarantee that we provide a complete and highly qualified assistance and that we meet the timing and control requirements of the process

List of services

Analysis of the documents provided and the indication of risks

Development of local documents and assistance in the development of documents according to the list

Development and design of layouts

Translation and notarization of documents

Registration stages

  1. Preparation and collection of documents

  2. Importation of product samples for expert examination

  3. Signing a contract with the state body

  4. Submission of a completed dossier to the state body

  5. Paying the invoice for laboratory testing

  6. Conducting of expert examinations and testings

  7. Passing the expert advisory body and obtaining an expert opinion and scientific report

  8. Obtaining a certificate of state registration and adding into the register

Service cost

State license fee

5 MCI (monthly calculation index)

The final cost and terms will be calculated at your request

Questions and Answers

1. How is the document calculated?

1. Why do medical devices undergo testing?

1. Is it possible to suspend or revoke the registration certificate of a medicine?

2. What is the period of registration of a medicine?

3. When is it not possible to conduct clinical or preclinical trials?

1. List of documents required for registration

1. List of documents required for registration

1. Which documents are required for registration?

1. Which documents on the status of pharmacovigilance activities are required to be submitted?

2. Are illustrations, images and graphics included in the calculation of a document?