# The Human Medicines Regulations 2012, Paragraph 4


The manufacturer must conduct all manufacture and assembly operations in such a way as to ensure that the medicinal products to which the UK marketing authorisation relates conform with the standards of strength, quality and purity applicable to them under the UK marketing authorisation.

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Source: https://www.legislation.gov.uk/uksi/2012/1916/schedule/9/paragraph/4 (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/schedule-9/paragraph-4
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.