Amendment of the Medicines for Human Use (Clinical Trials) Regulations 2004
This section has no associated Explanatory Memorandum
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;”.
(1)