The Medicines (Products for Human Use) (Fees) (Amendment) Regulations 2012

Type Statutory-Instrument
Publication 2012-10-04
Last updated 2013-04-01
State In force
Department King's Printer of Acts of Parliament
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Made: 4th October 2012

Laid before Parliament: 10th October 2012

Coming into force: 2nd November 2012

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Citation and commencement

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Amendment of the Medicines (Products for Human Use) (Fees) Regulations 2012

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Signed

Signed by authority of the Secretary of State for Health.

Dr Daniel Poulter — Parliamentary Under-Secretary of State, — 3rd October 2012

Edwin Poots — Minister for Health, Social Services and Public Safety — 2nd October 2012

David Evennett — Robert Goodwill — Two of the Lords Commissioners of Her Majesty's Treasury — 4th October 2012

Explanatory note

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Footnotes

[^f00001]: 1971 c.69; as amended by regulation 45(2) of S.I. 2008/2297 and section 21 of the Health and Medicines Act 1988 (c.49). By virtue of section 1(3) of the Medicines Act 1971 (“the 1971 Act”), expressions used in that section have the same meaning as in the Medicines Act 1968 (c.67) (“the 1968 Act”). See therefore section 1 of the 1968 Act, as substituted by paragraph 2 of Schedule 34 to the Human Medicines Regulations 2012 (S.I. 2012/1916) (“the 2012 Regulations”) which provides the meaning of the expression “the Ministers”, which is relevant to the powers being exercised in the making of these Regulations. By virtue of regulation 348 of, and paragraph 36 of Schedule 34 to, the 2012 Regulations, references in section 1(1) of the 1971 Act to an application for a licence, or for the variation or renewal of such a licence under Part 2 of the 1968 Act, shall have effect as a reference to any application under Parts 3 to 8 of the 2012 Regulations.

[^f00002]: In the case of the Secretary of State, by virtue of Article 2(1) of S.I. 1999/3142. In the case of the Minister for Health, Social Services and Public Safety, by virtue of section 95(5) of, and paragraph 10 of Schedule 12 to, the Northern Ireland Act 1998 (c.47); the Department for which the Minister is responsible was renamed by virtue of Article 3(6) of S.I. 1999/283 (N.I.1).

[^f00003]: 1972 c.68.

[^f00004]: 1973 c.51.

[^f00005]: See Article 2(1) of and Schedule 1 to the European Communities (Designation) Order 1972 (S.I. 1972/1811).

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

[^f00007]: S.I. 2012/504.

[^f00008]: This relates to Article 7 of Commission Regulation (EC) No 1234/2008 (OJ No L 334, 12.12.2008, p7) as amended by Commission Regulation (EU) No 712/2012 (OJ No L 209, 4.8.2012, p4).

Editorial notes

[^key-c588315f26883328a78bd5212fc3f405]: Regulations revoked (1.4.2013) by The Medicines (Products for Human Use) (Fees) Regulations 2013 (S.I. 2013/532), reg. 60(1) (with reg. 60(2)(3))

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