# 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, Article 118b

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

Member States shall organise meetings involving patients ‘ and consumers ’ organisations and, as necessary, Member States’ enforcement officers, in order to communicate public information about the actions undertaken in the area of prevention and enforcement to combat the falsification of medicinal products.

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Source: https://www.legislation.gov.uk/eudr/2001/83/article/118b (the official version)
Page: https://openlegislation.uk/eu-directive-2001-83/article-118b
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.