The Medicated Feedingstuffs and Feedingstuffs (Zootechnical Products) (Consequential Provisions) Regulations 1998
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The Secretary of State and the Minister of Agriculture, Fisheries and Food, being Ministers designated[1] for the purposes of section 2(2) of the European Communities Act 1972[2] in relation to medicinal products and the common agricultural policy of the European Community, acting jointly, in exercise of the powers conferred on them by the said section 2(2), hereby make the following Regulations: Title and commencement
Revocations and savings
(2) The revocation of the instruments at items
1 and 3 of Schedule 1 shall not have effect to prevent the provisions of:
(b) regulation 74(2) of the Feedingstuffs (Zootechnical Products)
Regulations 1998[4] from applying to matters to which
they would have applied had paragraph (1) not come into force.
3. The instruments listed in Schedule 2 are hereby amended in accordance with that Schedule. Sewel
1st April 1998
Jeff Rooker
9th April 1998
SCHEDULE 1 REVOCATIONS
SCHEDULE 2 AMENDMENTS
Amendment of 1988 Regulations
(ii) the following definitions shall be omitted - "appropriate non-proprietary name"; "approved name"; "approved synonym"; (iii) in the definition of "container", after the words "medicated feeding stuff" there shall be inserted the words ", intermediate product or zootechnical product"; (iv) in the definition of "dosage unit" the words "or excepted medicated feeding stuff shall" be omitted at both places where they occur; (v) the following definitions shall also be omitted - "data sheet"; "excepted medicated feeding stuff"; "expiry date"; "final medicated feeding stuff"; "foreign or international compendium of standards"; "intermediate medicated feeding stuff"; "international non-proprietary name"; (vi) immediately before the definition of "marketing authorisation"
there shall be inserted the following definition -
(ix) the following definitions shall also be omitted - "person responsible for the composition of the medicinal product or excepted medicated feeding stuff"; "prescription only medicine"; "proprietary designation"; (x) in the definition of "quantity", there shall be omitted the words ", excepted medicated feeding stuff"; and (xi) after the definition of "quantity", there shall be substituted
for all the remaining definitions the following definition -
(c) regulations 4, 5 and 7 shall be omitted; (d) for regulation 6 there shall be substituted the following regulation
-
6. - (1) Subject to paragraph (2) below, where a medicated feeding stuff, an intermediate product or a zootechnical product is for administration in a medicinal test on animals, every container and package of such feeding stuff or product shall be labelled with the words "For Animal Test Use Only" and to show the particulars set out in Schedule 4. (2) Where any container or any package enclosing
the container of -
(b) an intermediate product, or (c) a zootechnical product,
8. A person who, in the course of a business carried on by him, sells or supplies a medicated feeding stuff, an intermediate product or a zootechnical product for administration in a medicinal test on animals without its being enclosed in a container shall not be taken to contravene regulation 6 if a leaflet which complies with the requirements of regulation 6 is supplied with such feeding stuff or product and such leaflet is delivered to the purchaser or consignee with such feeding stuff or product.";
(ii) after the words "medicated feeding stuff", at each place where they occur, there shall be inserted the words ", intermediate product or zootechnical product"; and (iii) paragraphs (3), (7) and (8) shall be omitted;
(ii) the words "(not being an excepted medicated feeding stuff)"
shall be omitted;
(ii) in paragraph (b), after the words "medicated feeding stuffs"
there shall be inserted the words ", intermediate products or zootechnical
products";
(j) in regulation 13, the words from "or who contravenes" to "excepted medicated feeding stuffs" shall be omitted; (k) Schedules 1, 2 and 3 shall be omitted; and (l) in Schedule 4 -
PARTICULARS REQUIRED IN THE LABELLING OF CONTAINERS AND PACKAGES OF MEDICATED FEEDING STUFFS, INTERMEDIATE PRODUCTS OR ZOOTECHNICAL PRODUCTS FOR MEDICINAL TESTS ON ANIMALS"; (iii) in paragraphs 3, 4, 6, 8 and 9, after the words "medicated feeding stuff", in each place where they occur, there shall be inserted the words ", intermediate product or zootechnical product"; (iv) paragraph 5 shall be omitted; (v) in paragraph 7, sub-paragraph (a) shall be omitted and in sub-paragraph (b) the words "(not being an excepted medicated feeding stuff)" shall be omitted and the words ", intermediate product or zootechnical product" shall be inserted immediately after the words "feeding stuff" in each place where they survive; and (vi) in paragraph 9, for the words "regulation 6(3)" there shall be substituted the words "regulation 6(2)". Amendment of 1994 Regulations
(iiiB) in the case of an authorised medicated pre-mix, as so defined,
which falls within regulation 18(3), 21(3) or 28(4) of those Regulations,
the capital letters "MFSX";".
3. Paragraph 3 of Schedule 3 to the Medicines (Products for Animal Use - Fees) Regulations 1997[7] shall be omitted.
(This note is not part of the Regulations)
These Regulations make provision consequent on the making of the Medicated Feedingstuffs Regulations 1998 and the Feedingstuffs (Zootechnical Products) Regulations 1998. Regulation 2 and Schedule 1 revoke the Medicines (Feeding Stuffs Additives) Order 1975, S.I. 1975/1349, the Medicines (Exemption from Licences) (Intermediate Medicated Feedingstuffs) Order 1989, S.I. 1989/2325, the Medicines (Intermediate Medicated Feedingstuffs) Order 1989, S.I. 1989/2442, the Medicines (Exemption from Licences) (Intermediate Medicated Feedingstuffs) (Amendment) Order 1990, S.I. 1990/567, the Medicines (Medicated Animal Feedingstuffs) (No. 2) Regulations 1992, S.I. 1992/1520, the Medicines (Medicated Animal Feedingstuffs) (Amendment) Regulations 1994, S.I. 1994/1531, the Medicines (Medicated Animal Feedingstuffs) (Amendment) Regulations 1995, S.I. 1995/799, the Medicines (Medicated Animal Feedingstuffs) (Amendment) Regulations 1996, S.I. 1996/769 and the Medicines (Medicated Animal Feedingstuffs) (Amendment) Regulations 1997, S.I. 1997/638, subject to a saving in relation to S.I. 1975/1349 and S.I. 1989/2442. Regulation 3 and Schedule 2 amend the Medicines (Labelling of Medicinal Products for Incorporation in Animal Feeding Stuffs and of Medicated Animal Feeding Stuffs) Regulations 1988, S.I. 1988/1009, so that (with the exception of regulation 9) they apply only to the labelling of containers and packages of feed materials for administration in medicinal tests on animals. They also amend the product categorisation labelling requirement of the Marketing Authorisations for Veterinary Medicinal Products Regulations 1994, S.I. 1994/3142 and delete one provision from the Medicines (Products for Animal Use - Fees) Regulations 1997.
Notes: [1] S.I. 1972/811.back [2] 1972 c. 68.back [3] S.I. 1998/1046.back [4] S.I. 1998/1047.back [5] S.I. 1988/1009, relevant amending instruments are S.I. 1994/3142 and S.I. 1996/2194.back [6] S.I. 1994/3142 to which there are amendments not relevant to these Regulations.back [7] S.I. 1997/1469.back
ISBN 0 11 065994 3 |
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