Veterinary pre-submission Q&A: 1-20


This guidance only applies to procedures initiated under Directive 2001/82/EC and Regulation (EU) 726/2004 before 28 January 2022.

This page lists questions 1 to 20 of the European Medicines Agency's questions and answers on pre-submission guidance for veterinary medicinal products.

The page is updated regularly to reflect new developments, to include guidance on further pre-authorisation procedures and to reflect the implementation of new European legislation. New and revised topics are marked as “New” or “Rev.” on publication.

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