# The Human Medicines Regulations 2012, Paragraph 15


The provisions of this Part are standard provisions of a manufacturer's licence relating to the import of medicinal products from—
(a) in the case of an import into Great Britain, a country other than Northern Ireland or a country other than an approved country for import, or
(b) in the case of an import into Northern Ireland, a country other than an EEA State.

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Source: https://www.legislation.gov.uk/uksi/2012/1916/schedule/4/paragraph/15 (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/schedule-4/paragraph-15
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.