Legalize / United Kingdom / Statutory-Instrument

The Feedingstuffs (Zootechnical Products) and Medicated Feedingstuffs (Amendment) (England, Scotlandand Wales) Regulations 2005

Type Statutory-Instrument

Publication 2005-03-24

State In force

Department King's Printer of Acts of Parliament

Source legislation.gov.uk

Reform history JSON API PDF

Made: 24th March 2005

Laid before Parliament: 1st April 2005

Coming into force: 22nd April 2005

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Title, commencement and extent

1

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Amendment of the Feedingstuffs (Zootechnical Products) Regulations 1999

2

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Amendment of the Medicated Feedingstuffs Regulations 1998

3

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SCHEDULE

PART 1 — Substitution of the table in Part II of Schedule 3 to the Feedingstuffs (Zootechnical Products) Regulations 1999

Application for the approval of an establishment to manufacture a zootechnical—	Fee (£)
Notes If an application for an approval under regulation 10(1)(a) is made at the same time as an application relating to those premises for a manufacturer’s licence to manufacture a medicated premix under the Medicines Act 1968, no fee is payable under these Regulations. If premises used for manufacturing zootechnical compound feedingstuffs are inspected for an official check at the same time as they are inspected for the renewal of an approval under the MF Regulations, no fee is payable in relation to the zootechnical compound feedingstuffs. Where more than one of the manufacturing activities tabulated above is carried on at a premises, only one fee is payable, which shall be the higher (or, as the case may be, the highest).	Notes If an application for an approval under regulation 10(1)(a) is made at the same time as an application relating to those premises for a manufacturer’s licence to manufacture a medicated premix under the Medicines Act 1968, no fee is payable under these Regulations. If premises used for manufacturing zootechnical compound feedingstuffs are inspected for an official check at the same time as they are inspected for the renewal of an approval under the MF Regulations, no fee is payable in relation to the zootechnical compound feedingstuffs. Where more than one of the manufacturing activities tabulated above is carried on at a premises, only one fee is payable, which shall be the higher (or, as the case may be, the highest).
additive with a view to putting it into circulation under regulation 10(1)(a) or 12, or the annual fee covering official checks payable in respect of that establishment under regulation 75	866
premixture with a view to putting it into circulation under regulation 10(1)(b) or 12, or the annual fee covering official checks payable in respect of that establishment under regulation 75	866
compound feedingstuff with a view to putting it into circulation under regulation 10(1)(c) or 12, or the annual fee covering official checks payable in respect of that establishment under regulation 75	188
compound feedingstuff for the exclusive use of the applicant’s holding under regulation 10(1)(d) or 12, or the annual fee covering official checks payable in respect of that establishment under regulation 75	115
compound feedingstuff, using a minimum proportion of 0.05% by weight of a premixture, under regulation 10(1)(e) or 12, or the annual fee covering official checks payable in respect of that establishment under regulation 75	546

PART 2 — Substitution of the table in Part III of Schedule 3 to the Feedingstuffs (Zootechnical Products) Regulations 1999

Application/annual fee—	Fee (£)
for the approval to exercise an intermediary activity under regulation 18 or 20, or the annual fee covering official checks in respect of that intermediary under regulation 75	128

PART 3 — Substitution of the table in Part I of Schedule 1 to the Medicated Feedingstuffs Regulations 1998

Application for the grant or renewal of an approval of premises to manufacture—	Fee (£)
Note Where more than one of the manufacturing activities tabulated above is carried on at a premises, only one fee is payable, which shall be the higher (or, as the case may be, the highest).	Note Where more than one of the manufacturing activities tabulated above is carried on at a premises, only one fee is payable, which shall be the higher (or, as the case may be, the highest).
authorised intermediate products	546
medicated feedingstuffs incorporating medicated pre-mixes at any concentration	546
medicated feedingstuffs incorporating medicated pre-mixes at a concentration of 2kg per tonne or more only	365
medicated feedingstuffs incorporating medicated pre-mixes at a concentration of 2kg per tonne or more for the manufacturer’s own use	135

PART 4 — Substitution of the table in Part II of Schedule 1 to the Medicated Feedingstuffs Regulations 1998

Application—	Fee (£)
for the grant or renewal of a distributor’s approval	128

Signed

Ben Bradshaw — Parliamentary Under Secretary of State — Department for Environment, Food and Rural Affairs — 24th March 2005

Explanatory note

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Footnotes

[^f00001]: 1972 c. 68.

[^f00002]: S.I. 1972/1811.

[^f00003]: OJ No. L.31, 1.2.2002, p. 1.

[^f00004]: S.I. 1999/1871; relevant amending instruments are S.I. 2000/1686, 2002/696, 2003/545 and 2004/1036.

[^f00005]: S.I. 1998/1046; relevant amending instruments are S.I. 2000/1686, 2002/697, 2003/752 and 2004/1036.

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Editorial notes

[^key-023818c050e204665eed244ea022a99c]: Regulations revoked (1.1.2006) by The Veterinary Medicines Regulations 2005 (S.I. 2005/2745), Sch. 8 Pt. 2 (with Sch. 8 Pt. 4)

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