# 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 74

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

When new facts are brought to their attention, the competent authorities shall examine and, as appropriate, amend the classification of a medicinal product by applying the criteria listed in Article 71.

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Source: https://www.legislation.gov.uk/eudr/2001/83/article/74 (the official version)
Page: https://openlegislation.uk/eu-directive-2001-83/article-74
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.