# The Medicines for Human Use (Clinical Trials) Regulations 2004, Paragraph 14F


The holder of the authorisation shall ensure that the information in the MM (IMP) master file is kept up to date at all times.

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Source: https://www.legislation.gov.uk/uksi/2004/1031/schedule/7/paragraph/14F (the official version)
Page: https://openlegislation.uk/medicines-for-human-use-clinical-trials-regulations-2004/schedule-7/paragraph-14F
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.