1) The transitional period has been extended until December 31, 2030, allowing veterinary products registered in EAEU countries to continue their circulation throughout the Union.
During this period, there is also the possibility of registering products according to national legislation, which grants the right to sell them in specific EAEU states.
2) The possibility of circulating veterinary products in the Union market that were registered in member states before the new EAEU rules came into effect has been established.
Condition: the registration (or re-registration) of these products, as well as any changes to their registration files, must be confirmed after the rules come into effect but before the end of the transitional period.
3) A provision has been introduced for the mutual recognition of documents confirming that the production of veterinary medicines complies with the requirements of good manufacturing practice of the EAEU, which were issued by the authorized bodies of the member states.
Condition: the documents must be issued in accordance with the legislation of the countries concerning production facilities located in third countries, before the rules of the Union come into effect.
4) During the transitional period, the EEC will have the ability to compile a list of reference veterinary medicinal products with the possibility of editing it as necessary.
