Mass Media Publications


Classification of medical devices

Medical devices, depending on the degree of potential risk of harm to health during use, are divided into 4 classes.

Classes are indicated by numbers and letters: 1, 2a, 2b and 3. Each medical device belongs to only one class.


MedExpert on Medica 2019

MedExpert Company at the largest Healthcare Exhibition in Germany.



Dear colleagues, partners!

We hasten to inform you that MedExpert successfully passed the recertification audit, which was conducted by independent experts of the German organization TÜV SÜD. The company has once again confirmed the compliance of the quality of activities with the requirements of the international standard ISO 9001: 2015.


Rules of state registration, re-registration of drugs, medical devices and medical equipment

We inform you that since June 14, 2019, amendments to Order No. 735 of the Minister of Health of the Republic of Kazakhstan dated November 18, 2009 “On Approval of the Rules for State Registration, Re-registration and Amendments to the Registration File of Medicinal Products, Medical Products and Medical technology ".


Registration of perfumery and cosmetic products in the territory of the Member States of the Customs Union

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


Results of participation in the international dental exhibition KAZDENTEXPO-2019

From May 29 to May 31, a regular exhibition was held with the participation of our company.

KazDentExpo exhibition became the root cause of new acquaintances, pleasant and useful meetings, a storm of emotions and unforgettable memories.


Invitation to visit KAZDENTEXPO

Dear partners!

Group of companies “MedExpert” invites you to one of the largest international specialized dental exhibitions - KAZDENTEXPO.


Expert's review: Medical devices and medical equipment-related adverse events monitoring in the territory of the Republic of Kazakhstan.

The adverse events monitoring is a set of measures aimed at detecting, assessing, and analyzing adverse events, as well as making decisions about the safety, quality and efficiency of medical devices and medical equipment.


Expert's review: Advertising the medicines and medical products in the Republic of Kazakhstan.

Rules for advertising the medicines, medical products and medical equipment are regulated by the Order No. 105 dated February 27, 2015.


"Expert" category provides readers with information about the latest developments in the legislation of the Republic of Kazakhstan in the area of public health. Chief Physician Magazine, Number 3 (13), summer 2015

Order №227 dated 16.04.2015 approves the rules for labeling of medicines, medical devices and medical equipment.
Resolution №142 dated 02.24.2014 Standard for Public Service "The state registration, re-registration and variation of registration dossiers of medicinal products, medical devices and medical equipment".
Order №524 dated 26.06.2015 introduces amendments and additions to Order №736 dated 18.11.2009.
Order №523 dated 26.06.2015 introduces amendments and additions to Order №735 dated 18.11.2009.

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