Paragraph 6 Manufacturers' 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 manufacturer’s licence shall be £80 in respect of each variation applied for which consists of a change to the licence not requiring an inspection or medical, scientific or pharmaceutical assessment.