# The Human Medicines Regulations 2012, Paragraph 12


Where the product is authorised for sale or supply in Northern Ireland and is authorised under different names in different member States in accordance with Articles 28 to 39 of the 2001 Directive, a list of the names authorised in each member State.

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Source: https://www.legislation.gov.uk/uksi/2012/1916/schedule/27/paragraph/12 (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/schedule-27/paragraph-12
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.