# Directive 2009/35/EC of the European Parliament and of the Council of 23 April 2009 on the colouring matters which may be added to medicinal products (recast) (Text with EEA relevance), Article 1

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

Member States shall not authorise, for the colouring of medicinal products for human and veterinary use as defined in Article 1 of 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 and in Article 1 of Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use, any colouring matters other than those covered by Annex I to Directive 94/36/EC.

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Source: https://www.legislation.gov.uk/eudr/2009/35/article/1 (the official version)
Page: https://openlegislation.uk/eu-directive-2009-35/article-1
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.