# 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 111a

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

The Commission shall adopt detailed guidelines laying down the principles applicable to inspections referred to in Article 111.
Member States shall, in cooperation with the Agency, establish the form and content of the authorisation referred to in Articles 40(1) and 77(1), of the reports referred to in Article 111(3), of the certificates of good manufacturing practice and of the certificates of good distribution practices referred to in Article 111(5).

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Source: https://www.legislation.gov.uk/eudr/2001/83/article/111a (the official version)
Page: https://openlegislation.uk/eu-directive-2001-83/article-111a
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.