Regulation 11 Renewals of certain manufacturer’s licences

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

reg. 11(1) sum substituted by Medicines for Human Use and Medical Devices (Fees and Miscellaneous Amendments) 2000 reg. 4(5) Sch.
regs 10, 11 am by Medicines for Human Use and Medical Devices (Fees and Miscellaneous Amendments) 2001 reg 5(14), Schedule
regs.6,10,11, Sch.1, Pt.II, paras.1, Table, 5,6, Pt.III, paras.2,3. 6-12 amended by Medicines for Human Use and Medical Devices (Fees and Miscellaneous Amendments) 1999 reg.4(2), Sch.
reg 11 am by Medicines for Human Use and Medical Devices(Fees Amendments) 2003 reg 4(1), (9), Schedule
reg. 11(1) sum substituted by Medicines for Human Use and Medical Devices (Fees Amendments) 2004 reg. 15 Sch.
reg 11 am by Medicines for Human Use and Medical Devices (Fees Amendments) 2006 reg 2, schedule
reg 11 am by Medicines for Human Use and Medical Devices (Fees and Miscellaneous Amendments) 2002 reg 5(1), (9), Schedule

(1)

Subject to regulation 23, the fee payable in connection with an application for renewal of a manufacturer’s licence which is limited solely to the manufacture or assembly of medicinal products the sale or supply of which does not require a marketing authorization or a product licence and to which article 2(2)(i)(e) (exemptions for certain special manufactured products) of the Medicines (Exemption from Licences) (Special and Transitional Cases) Order 1971^f1 applies, shall be £85.

(2)

In respect of any inspection made in connection with an application referred to in paragraph (1), the fee payable shall be that prescribed in paragraph 2(d) of Schedule 2.

Annotations

Footnotes

f1: S.I. 1971/1450; to which there are amendments not relevant to these Regulations.