# 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, Article 87

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

Member States shall take appropriate measures to encourage veterinarians and other professionals concerned to report to the competent authorities any adverse reaction of veterinary medicinal products.

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Source: https://www.legislation.gov.uk/eudr/2001/82/article/87 (the official version)
Page: https://openlegislation.uk/eu-directive-2001-82/article-87
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.