The European Medicines Agency (EMA) is preparing scientific and technical recommendations to feed into delegated and implementing acts as part of the implementation of the Veterinary Medicines Regulation (Regulation (EU) 2019/6). EMA is providing these recommendations at the request of the European Commission.

Details on the European Commission's requests and EMA's recommendations are included below and are also available on the European Commission's website. 

EMA's recommendations are prepared by ad hoc experts groups composed of members of the European network of experts and EMA staff, in collaboration with other EU bodies, where necessary. 

EMA updates this page when new recommendations become available.

For more information on implementation of the Regulation, see Veterinary Medicinal Products Regulation.