# 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 18

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

Where a Member State is informed in accordance with Article 8(3)(1) that another Member State has authorised a medicinal product which is the subject of a marketing authorisation application in the Member State concerned, it shall reject the application unless it was submitted in compliance with Articles 28 to 39.

---
Source: https://www.legislation.gov.uk/eudr/2001/83/article/18 (the official version)
Page: https://openlegislation.uk/eu-directive-2001-83/article-18
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.