# The Human Medicines Regulations 2012, Paragraph 17


A document showing that the manufacturer of the medicinal product is authorised to produce medicinal products in the manufacturer's own country.

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Source: https://www.legislation.gov.uk/uksi/2012/1916/schedule/8/paragraph/17 (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/schedule-8/paragraph-17
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.