# Regulation (EU) 2019/6 of the European Parliament and of the Council of 11 December 2018 on veterinary medicinal products and repealing Directive 2001/82/EC (Text with EEA relevance), Division 10: In cases of applications for marketing authorisations for veterinary medicinal products indicated for animal species and indications representing smaller market sectors, a more flexible approach may be applicable. In such cases, relevant scientific guidelines and/or scientific advice should be taken into account.

Extent: E+W+S+N.I.

This Annex is divided in four titles:
Title I describes the standardised requirements for applications for veterinary medicinal products other than immunological veterinary medicinal products.
Title II describes the standardised requirements for applications for immunological veterinary medicinal products.
Title III describes specific types of marketing authorisation dossiers and requirements.
Title IV describes the dossier requirements for particular types of veterinary medicinal products.

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Source: https://www.legislation.gov.uk/eur/2019/6/annex/II/division/1/division/10 (the official version)
Page: https://openlegislation.uk/eu-regulation-2019-6/annex-II/division-1/division-10
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.