# The Medicines (Marketing Authorisations and Miscellaneous Amendments) Regulations 2004, Regulation 9: Amendment of the Medicines for Human Use (Clinical Trials) Regulations 2004


In the Medicines for Human Use (Clinical Trials) Regulations 2004, in regulation 2 (interpretation), in paragraph (1), for the definition of “the European Medicines Agency” substitute the following definition—
““the European Medicines Agency” means the European Medicines Agency established by Regulation (EC) No. 726/2004 of the European Parliament and of the Council laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency;”.

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Source: https://www.legislation.gov.uk/uksi/2004/3224/regulation/9 (the official version)
Page: https://openlegislation.uk/medicines-marketing-authorisations-and-miscellaneous-amendments-regulations-2004/regulation-9
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.