# Directive 2001/82/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to veterinary medicinal products, 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.

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Source: https://www.legislation.gov.uk/eudr/2001/82/annex/I/division/1/division/4 (the official version)
Page: https://openlegislation.uk/eu-directive-2001-82/annex-I/division-1/division-4
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.