# The Medicines for Human Use (Clinical Trials) Regulations 2004, Paragraph 9A


The holder of the authorisation shall only import EAMS medicinal products if and to the extent that such products are required for the Early Access to Medicines Scheme.

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Source: https://www.legislation.gov.uk/uksi/2004/1031/schedule/7/paragraph/9A (the official version)
Page: https://openlegislation.uk/medicines-for-human-use-clinical-trials-regulations-2004/schedule-7/paragraph-9A
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.