# The Human Medicines Regulations 2012, Paragraph 30


The licence holder must provide such information as may be requested by the licensing authority concerning the type and quantity of medicinal products which the licence holder handles, stores or distributes.

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Source: https://www.legislation.gov.uk/uksi/2012/1916/schedule/4/paragraph/30 (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/schedule-4/paragraph-30
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.