# 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 4

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

The manufacturing process shall comply with the requirements of Commission Directive 91/412/EEC laying down the principles and guidelines for veterinary medicinal products and with the principles and guidelines on Good Manufacturing Practice (GMP), published by the Commission in The rules governing medicinal products in the European Union, Volume 4.

---
Source: https://www.legislation.gov.uk/eur/2019/6/annex/II/division/1/division/4 (the official version)
Page: https://openlegislation.uk/eu-regulation-2019-6/annex-II/division-1/division-4
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.