# 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 113

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

For the purpose of implementing Article 112, Member States may require manufacturers of immunological products to submit to a competent authority copies of all the control reports signed by the qualified person in accordance with Article 51.

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Source: https://www.legislation.gov.uk/eudr/2001/83/article/113 (the official version)
Page: https://openlegislation.uk/eu-directive-2001-83/article-113
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.