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State registration of perfumes and cosmetic products in Kazakhstan

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State registration of perfumes and cosmetic products in Kazakhstan

State registration is a procedure during which the quality and safety of products that are in direct contact with the human body (for example, cosmetics, medical devices, dietary additives, etc.) are confirmed

Registration of perfumes and cosmetic products in the Customs Union is regulated by law TR CU 009/2011 “On the safety of perfumes and cosmetic products.” Key concepts, lists of documents, and other important aspects relating to the circulation and registration of perfumes and cosmetic products are provided in technical regulations and other regulatory documents

A certificate of state registration is required for the following types of goods:

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

Consulting

Adding changes to the registration certificate

Adding changes to the registration dossier

Preparation and collection of the registration dossier

Development and analysis of normative documentation

Collaboration with testing centers

Support in testing

Interaction with registration bodies

Registration stages

According to the current rules in the Republic of Kazakhstan, the registration of perfumes and cosmetic products includes the following stages:

  1. Collection of documentation and execution of all necessary documents

  2. Preliminary analysis, evaluation of the collected set of documents, and making amendments

  3. Preparation of the product samples and signing an agreement on testing

  4. Laboratory testing, recording, and reporting

  5. Submission of the collected set of documents together with the application to the registration body or certification body

  6. Making amendments if there are remarks

  7. Obtaining a certificate, declaration, and entering 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?