# The Human Medicines Regulations 2012, Paragraph 14D


The licence holder must maintain an MM master file for each MM medicinal product specified in the licence.

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