# The Human Medicines Regulations 2012, Paragraph 5


The licence holder must inform the licensing authority of any change that the licence holder proposes to make to a person named in the licence as—
(a) the person whose duty it is to supervise the manufacturing or assembling operations;
(b) in charge of the animals from which are derived substances used in the production of the medicinal products being manufactured or assembled; or
(c) responsible for the culture of living tissues used in the manufacture of the medicinal products being manufactured or assembled.

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Source: https://www.legislation.gov.uk/uksi/2012/1916/schedule/4/paragraph/5 (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/schedule-4/paragraph-5
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.