The Medicines for Human Use (Fees Amendments) Regulations 2006

Made: 26th July 2006

Laid before Parliament: 1st August 2006

Coming into force: 1st September 2006

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Citation, commencement and interpretation

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Amendment of regulation 2 of the of the General Fees Regulations

2

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Amendment of Schedule 1 to the General Fees Regulations

3

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Amendment of Schedule 3 to the General Fees Regulations

4

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Amendment of the Homoeopathic Regulations

5

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Signed

Signed by authority of the Secretary of State for Health

Andrew Burnham — Minister of State — 2006-07-20

Sealed with the Official Seal of the Department of Health, Social Services and Public Safety

Andrew McCormick — Permanent Secretary — 2006-07-21

Sealed with the Official Seal of the Department of Agriculture and Rural Development

Pat Toal — Permanent Secretary — 2006-07-26

We consent,

Alan Campbell — Dave Watts — Two of the Lords Commissioners of Her Majesty's Treasury — 2006-07-24

Explanatory note

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Footnotes

[^f00001]: 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 used in that section have the same meaning as in the Medicines Act 1968 (c. 67); see therefore section 1(1) of the 1968 Act, as amended by article 2(2) of, and Schedule 1 to, S.I. 1969/388, by article 5 of, and the Schedule to, S.I. 1999/3142, and by article 5(1) of, and paragraph 15 of Schedule 1 to, S.I. 2002/794, which contains a definition of “the Ministers” which is relevant to the powers being exercised in the making of these Regulations. See also regulation 9(12) of the Medicines for Human Use (Marketing Authorisations Etc.) Regulations 1994 (S.I. 1994/3144), by virtue of which the references in section 1(1) and (2)(b) of the 1971 Act to a licence under Part II of the 1968 Act include reference to a marketing authorization under the 1994 Regulations.

[^f00002]: In the case of the Secretary of State, by virtue of article 2(1) of, and paragraph 1 of the Schedule to, S.I. 1999/3142 and article 3(1)(c) and (7) of, and paragraph 15 of Schedule 1 to, S.I. 2002/794; and in the case of the Department of Health, Social Services and Public Safety and the Department of Agriculture and Rural Development, by virtue of the powers vested in the Ministers in charge of those Departments by virtue of section 95(5) of, and paragraph 10 of Schedule 12 to, the Northern Ireland Act 1998 (c. 47), which may now be exercised by the Departments by virtue of section 1(8) of, and paragraph 4(1)(b) of the Schedule to, the Northern Ireland Act 2000 (c. 1); the Departments were renamed by virtue of Article 3(4) and (6) of S.I. 1999/283 (N.I. 1).

[^f00003]: 1972 c. 68.

[^f00004]: 1973 c. 51.

[^f00005]: S.I. 1972/181.

[^f00006]: 1968 c. 67; section 129(6) was extended by section 1(3)(b) of the Medicines Act 1971.

[^f00007]: S.I. 1995/1116, as amended by S.I. 1996/683, 1998/574, 1999/566, 2000/592 and 3031, 2001/795, 2002/236 and 542, 2003/625 and 2321, 2004/666 and 1157, 2005/1124 and 2979, and 2006/494.

[^f00008]: S.I. 1994/105; relevant amending instruments are S.I. 1996/482, 2005/2753 and 2006/494.

[^f00009]: ()S.I. 1994/3144; see the definition of “the 1994 Regulations” in regulation 2(1) of the General Fees Regulations. Regulation 4(1B) was inserted by S.I. 2006/1952.

[^f00010]: Part III of Schedule 1 was amended by S.I.1996/683, 1998/574, 1999/566, 2000/592, 2001/795, 2002/236 and 542, 2003/625 and 2321, 2004/666 and 1157 and 2005/2979.

[^f00011]: See the definition of “Marketing Authorisation Regulations” in section 132(1) of the Medicines Act 1968 (c. 67), as inserted by S.I. 2005/1094.

[^f00012]: OJ No. L 297, 13.10.1992, p.8.

[^f00013]: See articles 1(5), 13 to 16, 53, 68, 69, 85, 100, 119 and 124.

Editorial notes

[^key-c913ad9bb040dff81d29af5c6b7f7594]: Regulations revoked (1.4.2013) by The Medicines (Products for Human Use) (Fees) Regulations 2013 (S.I. 2013/532), reg. 1(2), Sch. 9

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