# Regulation (EC) No 470/2009 of the European Parliament and of the Council of 6 May 2009 laying down Community procedures for the establishment of residue limits of pharmacologically active substances in foodstuffs of animal origin, repealing Council Regulation (EEC) No 2377/90 and amending Directive 2001/82/EC of the European Parliament and of the Council and Regulation (EC) No 726/2004 of the European Parliament and of the Council (Text with EEA relevance), Article 16: Administration of substances to food-producing animals

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

1. Only pharmacologically active substances which are classified in accordance with Article 14(2)(a), (b) or (c) may be administered to food-producing animals ....
2. Paragraph 1 does not apply in the case of clinical trials which are authorised under an Animal Test Certificate.

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Source: https://www.legislation.gov.uk/eur/2009/470/article/16 (the official version)
Page: https://openlegislation.uk/eu-regulation-2009-470/article-16
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.