# The Human Medicines Regulations 2012, Paragraph 13


(1) This paragraph applies in Northern Ireland where—
(a) a medicinal product which has undergone the controls referred to in paragraph 12A in a member State is imported to Northern Ireland; and
(b) each batch of the product is accompanied by control reports signed by another qualified person in respect of the medicinal product.
(2) Where this paragraph applies, the qualified person is not responsible for carrying out the controls referred to in paragraph 12A.

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Source: https://www.legislation.gov.uk/uksi/2012/1916/schedule/7/paragraph/13 (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/schedule-7/paragraph-13
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.