# The Human Medicines Regulations 2012, Regulation 17A: Manufacturing of MM medicinal products


A person may not manufacture or assemble an MM medicinal product unless—
(a) it is specified in a manufacturer’s licence (MM); and
(b) there is an MM master file relating to that product and it is manufactured or assembled in accordance with that master file.

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Source: https://www.legislation.gov.uk/uksi/2012/1916/regulation/17A (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/regulation-17A
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.