4. Where the trial is to be conducted at trial sites in [F1an] EEA State, a list of the competent authorities to which a request for authorisation has been made.U.K.
Textual Amendments
F1Word in Sch. 3 Pt. 2 para. 4 substituted (31.12.2020) by The Medicines for Human Use (Clinical Trials) (Amendment) (EU Exit) Regulations 2019 (S.I. 2019/744), regs. 1, 24(3)(b); 2020 c. 1, Sch. 5 para. 1(1)