# The Human Medicines Regulations 2012, Regulation 54: Applications relating to products in well-established medicinal use


(1) This regulation applies if an applicant for a UK marketing authorisation for a relevant medicinal product is able to demonstrate that the active substances of the product have been in well-established medicinal use within the United Kingdom or the European Union for at least 10 years, with recognised efficacy and an acceptable level of safety in terms of the conditions set out in Annex I to the 2001 Directive.
(2) The applicant may, by way of derogation from paragraph 10 of Schedule 8, replace the results of pre-clinical tests or clinical trials with appropriate scientific literature.

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Source: https://www.legislation.gov.uk/uksi/2012/1916/regulation/54 (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/regulation-54
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.