# The Human Medicines Regulations 2012, Paragraph 10


The results of the following in relation to the medicinal product and its constituent active substances—
(a) pharmaceutical (physico-chemical, biological or microbiological) tests;
(b) pre-clinical (toxicological and pharmacological) tests; and
(c) clinical trials.

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Source: https://www.legislation.gov.uk/uksi/2012/1916/schedule/8/paragraph/10 (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/schedule-8/paragraph-10
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.