# The Human Medicines Regulations 2012, Paragraph 14O


A POC master file must contain, as a minimum, the following information:
(a) the information specified in paragraph 1B(2) of Schedule 3; and
(b) the location of any POC sites at which manufacturing or assembly of the POC medicinal product has commenced, has been suspended or has ceased, the date on which manufacturing or assembly commenced or ceased, and the dates on which it was suspended.

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