Monthly report on application procedures, guidelines and related documents for veterinary medicines
This report provides current information related to the volume and evaluation of pre- and post-authorisation applications for medicinal products for veterinary use received by the European Medicines Agency (EMA) for the current and previous three years on:
• scientific advice requests;
• applications for initial evaluations, extensions, variations and renewals concerning marketing authorisations (MAs);
• applications for initial evaluations, extensions, modifications and extrapolations for maximum residue limits (MRLs);
• arbitration and referral procedures;
• requests for classification and re-classifications of products as Minor Use Minor Species (MUMS)/limited market.
