In order to ensure the originality of marked products in the product group "Medicinal Products," clause 4 of Resolution No. 149 dated 02.04.2022 "On the introduction of a mandatory digital marking system for medicinal products and medical devices" establishes a procedure according to which marking codes are provided directly to manufacturers, foreign holders of registration certificates, or their accredited representatives.
To obtain marking codes in the NIS "Asl Belgisi" system, the Holder of the medicinal product registration certificate or the accredited Representative of the registration certificate holder registers. Then, the registered User enters their Medicinal Products into the "National Catalog" subsystem and after successful moderation with the card status "Published," after the UOT, they can order marking codes and download them for application, sending them for application in production.
The manufacturer can also independently order marking codes using the integration of the NIS "Asl Belgisi" with the User's system. For this, the registered User of the NIS "Asl Belgisi" system provides the client token and OMS ID to the production site.
In turn, distributors register in the NIS "Asl Belgisi" system as a wholesale link. However, in this case, distributors also act as a kind of "importers." However, please note that the importer of medicinal products (local distributor) in the territory of the Republic of Uzbekistan must form the AIC, for which they need a list of marking codes of imported goods. That is, these are the codes they receive either from the foreign supplier or scan independently using a 2D scanner at the customs warehouse.
After completion of work on the part of the State Customs Committee, information about the marking codes will be included directly in the electronic cargo customs declaration (with subsequent automatic exchange with the marking system).
Currently, aggregation up to the box level is mandatory. If necessary, aggregation into pallets is also possible.
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