# The Human Medicines Regulations 2012, Paragraph 5


The manufacturer must maintain an effective pharmaceutical quality assurance system involving the active participation of the management and personnel of the different services involved.

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Source: https://www.legislation.gov.uk/uksi/2012/1916/schedule/9/paragraph/5 (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/schedule-9/paragraph-5
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.