1) The transitional period has been extended until December 31, 2030, allowing the use of veterinary products registered under the legislation of the EAEU member states throughout the Union.
During this time, there remains the possibility of registering products according to national legislation, which grants the right to use them in specific EAEU states.
2) Veterinary products registered in member states before the introduction of the new rules are also allowed in the Union market.
At the same time: it is necessary to confirm the registration (or re-registration) and changes in the registration file of these products after the introduction of the rules until the end of the transitional period.
3) A norm on mutual recognition of documents certifying the compliance of veterinary medicine production with the requirements of the EAEU good manufacturing practice rules, issued by the authorized bodies of the Union countries, has been established.
Condition: the documents must be issued in accordance with the legislation of the respective countries regarding production facilities located in third countries, before the rules of the Union come into effect.
4) During the transitional period, the EEC may compile and update a list of reference veterinary medicinal products as necessary.
