The Medicines (Fees Relating to Medicinal Products for Human Use) Amendment (No. 2) Regulations 1990
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MEDICINES The Medicines (Fees Relating to Medicinal Products for Human Use) Amendment (No. 2) Regulations 1990
1. These Regulations which may be cited as the Medicines (Fees Relating to Medicinal Products for Human Use) Amendment (No. 2) Regulations 1990, amend the Medicines (Fees Relating to Medicinal Products for Human Use) Regulations 1989[4] (hereinafter referred to as "the principal Regulations") and shall come into force for all purposes except those of regulations 3 and 8 on 18th December 1990 and for the purposes of regulations 3 and 8 on 1st January 1991.
2. For each amount specified in column (3) of the Schedule to these Regulations, where it appears in the provision of the principal Regulations specified in relation to it in column (1) of that Schedule (the subject matter of which is indicated in column (2) of that Schedule), there is substituted the amount specified in relation to it in column (4) of that Schedule.
3. Regulation 1(3) of the principal Regulations (exemption for National Health Service authorities) is hereby revoked.
4. In Schedule 1 to the principal Regulations (fees for applications, variations and renewals of licences), in paragraph 1 in Part I (interpretation), after the definition of "product licence (parallel import)", there shall be inserted the following
5.(1) In paragraph 2 of Part III of Schedule 1 to the principal Regulations (variations of manufacturers' licences), for the words "paragraph 4" there shall be substituted the words "paragraphs 4A and 5". (2) In paragraph 3 of Part III of Schedule 1 to the principal Regulations (variations of wholesale dealers' licences), for the words "paragraph 4" there shall be substituted the words "paragraphs 4B and 5". (3) For paragraph 4 of Part III of Schedule 1 to the principal Regulations (fees for applications for variations of licences) there shall be substituted the following "Other variations to Product Licences 4. The fee payable under regulation 6(a) of these Regulations in connection with an application for variation of a product licence shall be £100 in respect of each variation applied for which falls within one of the following paragraphs
Other variations to Manufacturers' Licences 4A. The fee payable under regulation 6(a) of these Regulations in connection with an application for variation of a manufacturer's licence shall be £100 in respect of each variation applied for which falls within one of the following paragraphs
Other variations to Wholesale Dealers' Licences 4B. The fee payable under regulation 6(a) of these Regulations in connection with an application for variation of a wholesale dealer's licence shall be £100 in respect of each variation applied for which falls within one of the following paragraphs
6. In Schedule 2 to the principal Regulations (fees for inspections)
7. In paragraph 3 of Schedule 3 to the principal Regulations (waiver, reduction or refund of fees)
8. Notwithstanding regulation 15(1) of the principal Regulations, where an application for the grant, variation or renewal of a licence or certificate under Part II of the Medicines Act 1968[6] is made before 1st April 1991 by an authority constituted under the National Health Service Act 1977[7], the National Health Service (Scotland) Act[8] or by a National Health Service trust[9], the fee payable in accordance with the other provisions of the principal Regulations in connection with the application shall be payable on 1st April 1991 and not at the time of the application.
Notes: [1] 1971 c. 69, as amended by section 21 of the Health and Medicines Act 1988 (c. 49); by virtue of section 1(3) of the 1971 Act expressions in that section have the same meaning as in the Medicines Act 1968 (c. 67), as amended by the Transfer of Functions (Wales) Order 1969 (S.I. 1969/388). The expression "the Ministers" is defined in section 1(1) of the 1968 Act as so amended. back [2] In the case of the Secretaries of State concerned with health in England and in Wales by virtue of article 2(2) of, and Schedule 1 to, the Transfer of Functions (Wales) Order 1969; in the case of the Secretary of State concerned with agriculture in Wales by virtue of article 2(3) of, and Schedule 1 to, the Transfer of Functions (Wales) (No. 1) Order 1978 (S.I. 1978/272); in the case of the Northern Ireland Departments by virtue of section 40 of, and Schedule 5 to, the Northern Ireland Constitution Act 1973 (c. 36) and section 1(3) of, and paragraph 2(1)(b) of Schedule 1 to, the Northern Ireland Act 1974 (c. 28). back [3] See section 129(6) of the Medicines Act 1968 (c. 67), as extended to include regulations made under the Medicines Act 1971 by section 1(3)(b) of that latter Act. back [4] S.I. 1989/418; the relevant amending instrument is S.I. 1990/210. back [5] S.I. 1971/972; the relevant amending instruments are S.I. 1972/1226 and 1977/1053. back [9] As established by orders made under section 5(1) of the National Health Service and Community Care Act 1990 (c. 19). back |
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