SCHEDULE 3 U.K. PARTICULARS AND DOCUMENTS THAT MUST ACCOMPANY AN APPLICATION FOR AN ETHICS COMMITTEE OPINION, A REQUEST FOR AUTHORISATION, A NOTICE OF AMENDMENT AND A NOTIFICATION OF THE CONCLUSION OF A TRIAL

PART 2 U.K. REQUEST FOR AUTHORISATION

4.  Where the trial is to be conducted at trial sites in [F1 an] EEA State, a list of the competent authorities to which a request for authorisation has been made. U.K.

Textual Amendments

F1 Word 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)