Marketing authorisation holders of veterinary medicinal products registered by national procedure, MRP, DCP or centralised procedure are required within electronic reporting of suspected adverse reaction related to these products; i.e. reporting via database EudraVigilance Veterinary, to act upon document „The Schemas for the Guidance on the Electronic Data Interchange of Safety Data for Veterinary Medicinal Products in the EU“. The document could be downloaded at the following web adress of the European Medicines Agency (EMA): http://eudravigilance.emea.europa.eu/veterinary/reporting.html