# The Human Medicines Regulations 2012, Regulation 74B: Obligation to provide information relating to methods of manufacture and control: POC medicinal products


The holder of a UK marketing authorisation relating to a POC medicinal product must provide the holder of the manufacturer’s licence (POC) relating to that product with information in order to enable the licence holder to ensure that the manufacturer’s licence (POC) and POC master file relating to the product are consistent with the marketing authorisation at all times.

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Source: https://www.legislation.gov.uk/uksi/2012/1916/regulation/74B (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/regulation-74B
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.