# The Human Medicines Regulations 2012, Paragraph 16


Details of any authorisation or registration obtained by the applicant in a country other than the United Kingdom allowing the medicinal product to be placed on the market.

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Source: https://www.legislation.gov.uk/uksi/2012/1916/schedule/12/paragraph/16 (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/schedule-12/paragraph-16
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.