Paragraph 3 Product licences

Changes not yet applied. Later legislation changes this provision in ways not yet written into the text below:

Sch.1, Pt III, para l(aa) added by Medicines (Products for Human Use—Fees) 1994 reg.7(4)(a)
Sch.1, Pt III, para 1(b) amended by Medicines (Products for Human Use—Fees) 1994 reg.2, Sch
Sch.1, Pt III, para 2 amended by Medicines (Products for Human Use—Fees) 1994 reg.7(4)(b)
Sch.1, Pt III, para 2A added by Medicines (Products for Human Use—Fees) 1994 reg.7(4)(c)
Sch.1, Pt III, paras 4, 5(a)(b), 6-10 amended by Medicines (Products for Human Use—Fees) 1994 reg.2, Sch
Sch.1 substituted by Medicines (Products for Human Use– Fees) 1992 reg.8(2)(c)
Sch.1, Pt I. para l(n), head (defn of complex application) substituted by Medicines (Products for Human Use– Fees) 1992 reg.8(2)(a)
Sch.1, Pt l(n). head (v) added by Medicines (Products for Human Use– Fees) 1992 reg.8(2)(b)
Sch.1, Pt III, paras l(a)(b), 4, 5(b), 9 amended by Medicines (Products for Human Use– Fees) 1992 Sch

The fee payable under regulation 7(a) in connection with an application for variation of a product licence (parallel import) which is a complex application, shall be the same as that payable in connection with an application for the grant of such a licence as specified in paragraph 1 of Part II of this Schedule.