# The Human Medicines Regulations 2012, Paragraph 14J


The licence holder must keep under review the arrangements for supervision and control of the manufacture or assembly operations at each modular unit and, if the arrangements are found to be inadequate, ensure that appropriate remedial action is taken as soon as reasonably practicable.

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Source: https://www.legislation.gov.uk/uksi/2012/1916/schedule/4/paragraph/14J (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/schedule-4/paragraph-14J
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.

