# The Human Medicines Regulations 2012, Paragraph 14G


The licence holder must ensure that the information contained in the MM master file is kept up to date, and consistent with any UK marketing authorisation for the product, at all times.

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