# The Human Medicines Regulations 2012, Regulation 17B: Manufacturing of POC medicinal products


A person may not manufacture or assemble a POC medicinal product unless—
(a) it is specified in a manufacturer’s licence (POC); and
(b) there is a POC 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/17B (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/regulation-17B
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.