The Medicines (Products for Human Use) (Fees) Regulations 2016

Amendment of the Medicines for Human Use (Clinical Trials) Regulations 2004U.K.

This section has no associated Explanatory Memorandum

61.—(1) The Medicines for Human Use (Clinical Trials) Regulations 2004 F1 are amended as follows.

(2) In regulations—

(a)17(2)(b)(ii) (request for authorisation to conduct a clinical trial);

(b)24(10) (amendments by the sponsor);

(c)38(3)(b) (application for manufacturing authorisation); and

(d)44(8) (variation of manufacturing authorisation)

for “Medicines (Products for Human Use) (Fees) Regulations 2013” substitute “ Medicines (Products for Human Use) (Fees) Regulations 2016 ”.

Textual Amendments

F1S.I. 2004/1031; relevant amendments are made by S.I. 2006/1928 and 2013/532.