# 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 8: Study of residues

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

For immunological veterinary medicinal products, it will normally not be necessary to undertake a study of residues. However, where adjuvants and/or preservatives are used in the manufacture of immunological veterinary medicinal products, consideration shall be given to the possibility of any residue remaining in the foodstuffs. If necessary, the effects of such residues shall be investigated.
A proposal for a withdrawal period shall be made and its adequacy shall be discussed in relation to any residue studies which have been undertaken.

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Source: https://www.legislation.gov.uk/eudr/2001/82/annex/I/title/II/part/3/division/B/division/8 (the official version)
Page: https://openlegislation.uk/eu-directive-2001-82/annex-I/title-II/part-3/division-B/division-8
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.