# The Human Medicines Regulations 2012, Paragraph 1


A copy of the application submitted in connection with the granting of the ... UKMA(NI) which authorises the sale or supply of the medicinal product in Northern Ireland.

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Source: https://www.legislation.gov.uk/uksi/2012/1916/schedule/8C/paragraph/1 (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/schedule-8C/paragraph-1
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.