Veterinary drug manufacturers are advised to update their registration dossiers for the EAEU.

This was stated by Vasilina Gritsyuk, Deputy Director of the All-Russian State Center for Quality and Standardization of Veterinary Medicines and Feed (VGNKI, Rosselkhoznadzor ). She noted that many registration dossiers were prepared long ago, when different requirements were in effect , so additional research and updating of some data is necessary.

To determine what exactly needs to be improved, manufacturers can request methodological assistance by sending a letter to the center and submitting the required documents. In anticipation of the unification of EAEU requirements , documentation updates must be completed during the transition period of 2027, but the possibility of extending this deadline to 2030 is being discussed. This is due to the lack of preparedness among businesses and authorized bodies in the participating countries for the new requirements.