top of page

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.



Today's News
Follow us
  • LinkedIn Social Icon
  • Vimeo Social Icon
Newsletter on Pharma Legislation
the newsletter of
bottom of page