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


An MM (IMP) master file shall contain, as a minimum, the following information:
(a) the information specified in paragraph 10 of Schedule 6; and
(b) the location of any modular units at which manufacturing or assembly of the MM investigational medicinal product has commenced, has been suspended or has ceased, and the date on which manufacturing or assembly commenced, the dates on which it is suspended, or the date from which it has ceased.

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