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Statutory Instrument 2005 No. 1033The Feedingstuffs (Zootechnical Products) and Medicated Feedingstuffs (Amendment) (England, Scotlandand Wales) Regulations 2005(The document as of February, 2008) STATUTORY INSTRUMENTS2005 No. 1033AGRICULTUREThe Feedingstuffs (Zootechnical Products) and Medicated Feedingstuffs (Amendment) (England, Scotlandand Wales) Regulations 2005
The Secretary of State for Environment, Food and Rural Affairs, being designated for the purposes of section 2(2) of the European Communities Act 1972[1] in relation to the common agricultural policy of the European Community[2], in exercise of the powers conferred upon her by the said section 2(2), and having carried out the consultation required by Article 9 of Regulation (EC) No. 178/2002 of the European Parliament and of the Council laying down the general principles and requirements of food law, establishing the European Food Safety Authority and laying down procedures in matters of food safety[3], hereby makes the following Regulations: Title, commencement and extent 1.These Regulations may be cited as the Feedingstuffs (Zootechnical Products) and Medicated Feedingstuffs (Amendment) (England, Scotland and Wales) Regulations 2005, shall extend to England, Scotland and Wales and shall come into force on 22nd April 2005. Amendment of the Feedingstuffs (Zootechnical Products) Regulations 1999 2. - (1) The Feedingstuffs (Zootechnical Products) Regulations 1999[4] shall be amended in accordance with this regulation. (2) In regulation 2(1), for the definition of "the MF Regulations", substitute -
(3) In Schedule 3 -
(b) for the table in Part III, substitute that in Part 2 of the Schedule to these Regulations. Amendment of the Medicated Feedingstuffs Regulations 1998
(3) In Schedule 1 -
(b) for the table in Part II, substitute that in Part 4 of the Schedule to these Regulations.
Fees payable in relation to the approval and official checks of establishments
Notes 1.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. 2.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. 3.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). Fees payable in relation to the approval and official checks of intermediaries
Fees payable in relation to the grant or renewal of approvals of premises
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). Fees payable in relation to the grant or renewal of approvals of distributors
(This note is not part of the Order) These Regulations amend the Feedingstuffs (Zootechnical Products) Regulations 1999 (S.I. 1999/1871) and the Medicated Feedingstuffs Regulations 1998 (S.I. 1998/1046) in relation to England, Scotland and Wales. The Feedingstuffs (Zootechnical Products) Regulations 1999 implement in relation to zootechnical feedingstuffs a number of Community instruments including Council Directive 95/69/EC (OJ No. L 332, 30.12.95, p. 15) laying down the conditions and arrangements for the approval and registration of establishments and intermediaries operating in the animal feed sector. The first effect of the amendments made by these Regulations (regulation 2(2) and Parts 1 and 2 of the Schedule) is to raise the level of fees charged under the Feedingstuffs (Zootechnical Products) Regulations 1999 for applications and subsequent official checks in respect of establishments for which approvals are sought and held for the various activities that the manufacture and production of zootechnical feedingstuffs involves. The Medicated Feedingstuffs Regulations 1998 implement Council Directive 90/167/EEC (OJ No. L 92, 7.4.90, p. 42) laying down the conditions governing the preparation, placing on the market and use of medicated feedingstuffs in the Community. The second effect of the amendments made by these Regulations (regulation 3(2) and Parts 3 and 4 of the Schedule) is to raise the level of fees charged under the Medicated Feedingstuffs Regulations for applications and subsequent official checks in respect of establishments for which approvals are sought and held for the various activities that the manufacture, production and distribution of medicated feedingstuffs involves. The changes are itemised in the table below. A Regulatory Impact Assessment has been prepared and a copy has been placed in the library of each House of Parliament. Copies may be obtained from the Veterinary Medicines Directorate, Woodham Lane, New Haw, Addlestone, Surrey, KT15 3LS. Notes: [1]1972 c.68.back [2]S.I. 1972/1811.back [3]OJ No. L.31, 1.2.2002, p. 1.back [4]S.I. 1999/1871; relevant amending instruments are S.I. 2000/1686, 2002/696, 2003/545 and 2004/1036.back [5]S.I. 1998/1046; relevant amending instruments are S.I. 2000/1686, 2002/697, 2003/752 and 2004/1036.back ISBN0 11 072748 7 -- Back --
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