# The Human Medicines Regulations 2012, Paragraph 12B


In the case of an MM medicinal product or a POC medicinal product, the obligations in paragraphs 12(1)(a) and 12A(1)(a) may be satisfied by securing that each product has been manufactured and checked in accordance with these Regulations and the requirements of the marketing authorisation relating to the product.

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Source: https://www.legislation.gov.uk/uksi/2012/1916/schedule/7/paragraph/12B (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/schedule-7/paragraph-12B
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.