9. In the Medicines for Human Use (Clinical Trials) Regulations 2004(1), 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;”.