Approval of advertising materials

Blitz Medica LLP undertakes the collection, processing and preparation of advertising materials, as well as accompanies this process in the Republican State Enterprise on the right of economic management “National Center of Expertise of drug products, medical devices and medical equipment” before issuing a favorable conclusion. An obligatory condition for issuing permission to advertise drug products, medical devices and medical equipment is the preliminary examination of the advertising material in the state expert organization.

The permission for advertising is issued for the period of validity of the registration certificate of drug products, medical devices and medical equipment in accordance with Annex 2 to the Standard of State Service “Issuance of permission for advertising of drug products, medical devices and medical equipment” approved by the Resolution of the Government of the Republic of Kazakhstan dated October, 8, 2012 No. 1262.

The advertised properties and characteristics of drug products, medical devices and medical equipment, regardless of the type of advertising, must comply with the instructions for medical use approved by the authorized body at state registration, the operational document for medical equipment.

Drug products, medical devices and medical equipment distributed as advertising samples must be registered in the Republic of Kazakhstan and be accompanied by instructions for medical use, the operational document (for medical equipment).