According to the established deadlines, by December 31, 2025, previously registered products must be adapted in accordance with international obligations and the legislative acts of the EAEU.
As stated in the regulations on the import of medicinal products into the EAEU, for placing registered products under customs procedures (including release for domestic consumption, processing, re-import, and abandonment in favor of the state), it is necessary to provide the customs authority with information about the inclusion of the product in the register of registered medicinal products of the EAEU or in the local register of the EAEU member state.
For the release of products, the presence of a valid entry in the register is mandatory.
