# The Medicines for Human Use (Clinical Trials) Regulations 2004, Part 2: PROVISIONS WHICH MAY BE INCORPORATED IN AN AUTHORISATION RELATING TO THE MANUFACTURE OR ASSEMBLY OF INVESTIGATIONAL MEDICINAL PRODUCTS

Extent: E+W+S+N.I.



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Source: https://www.legislation.gov.uk/uksi/2004/1031/schedule/7/part/2 (the official version)
Page: https://openlegislation.uk/medicines-for-human-use-clinical-trials-regulations-2004/schedule-7/part-2
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.