The Animals, Meat and Meat Products (Examination for Residues and Maximum Residue Limits) (Amendment) Regulations 1994

Amendments

2.—(1) The principal Regulations shall be amended in accordance with the following provisions of this regulation and any reference in those provisions to any specified provision shall, unless the context otherwise requires, be taken to be a reference to the provision so specified in the principal Regulations.

(2) In paragraph (1) of regulation 2—

(a) after the definition of “animal test certificate” there shall be inserted the following definition—

““Annex IV substance” means a substance specified in Annex IV to the Council Regulation;”;

(b) for the definition of “approved laboratory” there shall be substituted—

““approved laboratory” means—

(a)

a laboratory approved by the appropriate Minister for the purposes of Council Directive 86/469/EEC(1); or

(b)

any laboratory under the direction or control of a public analyst appointed in accordance with section 27 of the Food Safety Act 1990;”;

(c) after the definition of “carcase” there shall be inserted—

““the Council Regulation” means the Regulation specified in Schedule 1;”;

(d) in the definition of “enforcement authority”, for the numbers “9, 10, 11”, in both places where they occur, there shall be substituted the numbers “13, 14, 15”;

(e) in the definition of “maximum residue limit”,

(i) for paragraph (a) there shall be substituted—

“(a) in respect of any substance specified in the first column of Annex I or Annex III to the Council Regulation, the limit specified in the fourth column opposite the reference to that substance and the applicable animal species specified in the third column, where the substance is contained in the part of the animal specified opposite it in the fifth column or in any meat or meat product derived from that part of the animal;”;

(ii) immediately after paragraph (b) there shall be inserted—

“and,

(c) in respect of each substance specified in column (1) of Schedule 4, the limit specified in column (2) thereof opposite the reference to such substance and the applicable animal species specified in column (5) where such substance is contained in that part of the animal specified in column (3) thereof opposite the reference to such substance or in any meat or meat product derived from that part of the animal;”.

(3) For paragraph (2) of regulation 2 there shall be substituted the following—

“For the purpose of ascertaining whether the maximum residue limit has been exceeded for the purposes of these Regulations, the presence of—

(a) the drug or drug metabolite (or combination thereof) specified in column (4) of Schedule 4 opposite the reference to each substance specified in column (1) of that Schedule shall be taken to indicate the presence of that substance in that part of an animal, or in any meat or meat product derived from that part of an animal, specified in column (3) of that Schedule opposite the reference to that substance and the maximum residue limit specified in column (2) of that Schedule opposite the reference to that substance shall then apply in respect of the presence in such part of an animal, or in any meat or meat product derived from such part of an animal, of any such drug or drug metabolite (or combination thereof) as if it were that substance; and

(b) the drug or drug metabolite (or combination thereof) specified in the second column of Annex I or III to the Council Regulation opposite the reference to each substance specified in the first column of those Annexes shall be taken to indicate the presence of that substance in that part of an animal, or in any meat or meat product derived from that part of an animal, specified in the fifth column of such Annex I or III, opposite the reference to that substance and the maximum residue limit specified in the fourth column of such Annex I or III opposite the reference to that substance shall then apply in respect of the presence in such part of an animal, or in any meat or meat product dervied from such part of an animal, of any such drug or drug metabolite (or combination thereof) as if it were that substance.”.

(4) In paragraph (1) of regulation 4, after the word “below,” there shall be inserted the words “and to regulation 4A below,”.

(5) After regulation 4 there shall be inserted—

“Prohibition on administration to animals of Annex IV substances.

4A.— (1) Subject to paragraph (2) below, no person shall administer to an animal any Annex IV substance.

(2) Nothing in regulation 4 above or paragraph (1) above shall prohibit giving an animal feeding-stuff containing an Annex IV substance (whether or not it is also an unlicensed substance) where that substance has been incorporated in accordance with Council Directive 70/524/EEC(2) as amended(3) concerning additives in feeding stuffs.”.

(6) In regulation 6, after the words “regulation 18” there shall be inserted “or any Annex IV substance”.

(7) The following sub-paragraph shall be inserted after regulation 8(1)(c)—

“(cc) an Annex IV substance;”.

(8) In regulations 13 and 14(1) after the word “substance”, in the second place where it occurs, there shall be inserted the words “or of an Annex IV substance”.

(9) In paragraph (2) of regulation 15, after the word “substance”, in the second place where it occurs, there shall be inserted the words “or Annex IV substance”.

(10) In paragraph (4) of regulation 15 and in regulation 17(5), after the word “contains” there shall be inserted the words “an Annex IV substance, or”.

(11) The following paragraphs shall be added at the end of regulation 20—

“(4) Subject to paragraph (5) below if an authorised officer directs a person to produce for inspection a record which paragraph (1) or (2) above requires him to keep, he shall comply with the direction.

(5) No direction may be given under paragraph (4) above after the end of the period mentioned in paragraph (3) above.

(6) The requirements under paragraphs (1) and (2) above to keep records in a permanent and legible form are not to be taken to prevent their being kept by means of computer.

(7) Where a record is so kept, the duty under paragraph (3) above to produce it for inspection, is a duty to produce it in a form in which it can be taken away.”.

(12) For Schedule 1 there shall be substituted—

Regulations 2(1) and (2)

“SCHEDULE 1 THE COUNCIL REGULATION

Official Journal of the Communities: References

Council Regulation (EEC) No. 2377/90 laying down a Community procedure for the maximum residue limits of veterinary medicinal products in foodstuffs of animal origin as amended by—	OJ No. L244, 18.8.90, p.1.
(a) Commission Regulation (EEC) No. 675/92	OJ No. L73, 19.3.92, p.8.
(b) Commission Regulation (EEC) No. 3093/92	OJ No. L311, 28.10.92, p.18.
(c) Commission Regulation (EEC) No. 895/93	OJ No. L93, 17.4.93, p.10.
(d) Council Regulation (EEC) No. 2901/93	OJ No. L264, 23.10.93, p.1.
(e) Commission Regulation (EC) No. 3425/93	OJ No. L312, 5.12.93, p.12.
(f) Commission Regulation (EC) No. 3426/93	OJ No. L312, 15.12.93, p.15.
(g) Commission Regulation (EC) No. 955/94	OJ No. L108, 29.4.94, p.8.
(h) Commission Regulation (EC) No. 1430/94	OJ No. L156, 23.6.94, p.6.”

(13) After Schedule 3 the following Schedule shall be inserted—

Regulations 2(1) and (2)

“SCHEDULE 4 MAXIMUM RESIDUE LIMITS

Column 1	Column 2	Column 3	Column 4	Column 5
Substance	Maximum residue limit	Part of the animal	Indicator residue	Animal species
Streptomycin	1,000 μg/kg	Any edible tissues	parent drug(4)	All food producing species
Clenbuterol	0.5 μg/kg	Any edible tissues	parent drug	All food producing species”

(1)

OJ No. L275, 26.9.86, p.36.

(2)

OJ No. L270, 14.12.70, p.1.

(3)

The relevant amendment is Council Directive 84/587/EEC (OJ No. L319, 8.12.84, p.13).

(4)

“parent drug” is referred to in the Council Regulation, see Annexes I and III.