# 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 1

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

The particulars and documents accompanying an application for marketing authorisation pursuant to Articles 12 to 13d shall be presented in accordance with the requirements set out in this Annex and shall take into account the guidance published by the Commission in The rules governing medicinal products in the European Union , Volume 6 B, Notice to applicants, Veterinary medicinal products, Presentation and Contents of the Dossier.

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