# 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, Division: Module 3

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

The provisions of Module 3, including compliance with monograph(s) of the European Pharmacopoeia, shall apply to the authorisation of herbal medicinal products. The state of scientific knowledge at the time when the application is lodged shall be taken into account.
The following aspects specific to herbal medicinal products shall be considered:

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Source: https://www.legislation.gov.uk/eudr/2001/83/annex/I/part/III/division/4/division/1 (the official version)
Page: https://openlegislation.uk/eu-directive-2001-83/annex-I/part-III/division-4/division-1
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.