# The Human Medicines Regulations 2012, Paragraph 1


The manufacturer must provide and maintain such staff, premises and plant as are necessary for the carrying out in accordance with the UK marketing authorisation of such stages of the manufacture and assembly of the medicinal products to which the authorisation relates as are undertaken by the manufacturer.

---
Source: https://www.legislation.gov.uk/uksi/2012/1916/schedule/9/paragraph/1 (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/schedule-9/paragraph-1
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.