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


The holder of the authorisation shall maintain and make available on request of the licensing authority an MM (IMP) master file for each MM investigational medicinal product to which the authorisation relates.

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