# 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 5

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

All information which is relevant to the evaluation of the veterinary medicinal product concerned shall be included in the application, whether favourable or unfavourable to the product. In particular, all relevant details shall be given of any incomplete or abandoned test or trial relating to the veterinary medicinal product.

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Source: https://www.legislation.gov.uk/eudr/2001/82/annex/I/division/1/division/5 (the official version)
Page: https://openlegislation.uk/eu-directive-2001-82/annex-I/division-1/division-5
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.