# The Medicines for Human Use (Clinical Trials) Regulations 2004, Paragraph 3


The holder of the authorisation shall provide such information as may be requested by the licensing authority concerning the type and quantity of any investigational medicinal products or EAMS medicinal products which he imports.

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Source: https://www.legislation.gov.uk/uksi/2004/1031/schedule/7/part/3/paragraph/3 (the official version)
Page: https://openlegislation.uk/medicines-for-human-use-clinical-trials-regulations-2004/schedule-7/part-3/paragraph-3
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.