# The Human Medicines Regulations 2012, Paragraph 18


The licence holder must provide such information as may be requested by the licensing authority concerning the type and quantity of any medicinal products which the licence holder imports.

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Source: https://www.legislation.gov.uk/uksi/2012/1916/schedule/4/paragraph/18 (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/schedule-4/paragraph-18
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.