# 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 G: OTHER INFORMATION

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

Information relating to the quality of the veterinary medicinal product not covered in the previous sections may be included in the dossier.
For medicated premixes (products intended for incorporation into medicated feedingstuffs), information shall be provided on inclusion rates, instructions for incorporation, homogeneity in-feed, compatibility/suitable feedingstuffs, stability in-feed, and the proposed in-feed shelf life. A specification for the medicated feedingstuffs, manufactured using these pre-mixes in accordance with the recommended instructions for use shall also be provided.

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Source: https://www.legislation.gov.uk/eudr/2001/82/annex/I/title/I/part/2/division/G (the official version)
Page: https://openlegislation.uk/eu-directive-2001-82/annex-I/title-I/part-2/division-G
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.