EMA contributed to discussions on implementing and delegated acts, which the European Commission prepared as part of the implementation of the Regulation. In particular, the Agency provided scientific and technical recommendations as and when requested by the European Commission.

EMA was also responsible for:

• revising its procedures and regulatory and scientific guidance documents, in line with the Regulation and its implementing and delegated acts;
• leading the implementation of Information technology (IT) systems required by the Regulation, including the Union Product Database, which serves as a single source of information on all authorised veterinary medicines and their availability in EU Member States;
• implementing the outcomes of the implementing and delegated acts.