# 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 6

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

The dose to be used shall be the quantity of the product to be recommended for use and the batch used for efficacy testing shall be taken from a batch or batches produced according to the manufacturing process described in Part 2 of the application.

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Source: https://www.legislation.gov.uk/eudr/2001/82/annex/I/title/II/part/4/chapter/II/division/A/division/6 (the official version)
Page: https://openlegislation.uk/eu-directive-2001-82/annex-I/title-II/part-4/chapter-II/division-A/division-6
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.