# The Human Medicines Regulations 2012, Paragraph 2


The manufacturer must provide and maintain such staff, premises, equipment and facilities for the handling, storage and distribution of the medicinal products to which the UK marketing authorisation relates and which the manufacturer handles, stores or distributes as are necessary to avoid deterioration of the medicinal products.

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Source: https://www.legislation.gov.uk/uksi/2012/1916/schedule/9/paragraph/2 (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/schedule-9/paragraph-2
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.