# 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 4: Identification and assay of adjuvants

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

Insofar as testing procedures are available, the quantity and nature of the adjuvant and its components shall be verified on the finished product.

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Source: https://www.legislation.gov.uk/eudr/2001/82/annex/I/title/II/part/2/division/E/division/4 (the official version)
Page: https://openlegislation.uk/eu-directive-2001-82/annex-I/title-II/part-2/division-E/division-4
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.