# The Medicines for Human Use (Clinical Trials) Regulations 2004, Paragraph 7


A description of the arrangements for the identification and storage of materials and ingredients before and during manufacture and for the storage of investigational medicinal products after manufacture, assembly or importation.

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Source: https://www.legislation.gov.uk/uksi/2004/1031/schedule/6/paragraph/7 (the official version)
Page: https://openlegislation.uk/medicines-for-human-use-clinical-trials-regulations-2004/schedule-6/paragraph-7
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.