# Regulation (EU) 2019/6 of the European Parliament and of the Council of 11 December 2018 on veterinary medicinal products and repealing Directive 2001/82/EC (Text with EEA relevance), 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/eur/2019/6/annex/II/title/II/part/2/division/E/division/4 (the official version)
Page: https://openlegislation.uk/eu-regulation-2019-6/annex-II/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.