The Medicines for Human Use (Clinical Trials) Regulations 2004 No. 1031

SCHEDULE 6 U.K. PARTICULARS THAT MUST ACCOMPANY AN APPLICATION FOR A MANUFACTURING AUTHORISATION

[F1 2.   A statement describing the types of investigational medicinal product in respect of which the authorisation is required, including their pharmaceutical forms.] U.K.

Textual Amendments

F1 Sch. 6 para. 2 substituted (29.8.2006) by The Medicines for Human Use (Clinical Trials) Amendment Regulations 2006 (S.I. 2006/1928), regs. 1(1), 31(a)