S.I. No. 183/2009 - European Communities (Control of Animal Remedies and their Residues) Regulations 2009

Type Statutory Instrument
Publication 2009-05-15
Last updated 2013-09-24
State In force superseded text
Text As published
articles 35

This is the act as published. Later amendments are not folded into the text below: each one is a separate act in this repository and an entry in this law's history.

2 amending acts · 2013-09-24, S.I. No. 361/2013 - European Union (Food Safety and Veterinary) (Accession of Croatia) Re…

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Notice of the making of this Statutory Instrument was published in

“Iris Oifigiúil” of 15th May, 2009.

I, BRENDAN SMITH, Minister for Agriculture, Fisheries and Food, in exercise of the powers conferred on me by section 3 of the European Communities Act, 1972 (No. 27 of 1972), for the purpose of giving effect to Council Directive 96/22/EC 1 of 29 April 1996, as amended by Directive 2003/74/EC 2 of the European Parliament and of the Council of 22 September 2003 and Directive 2008/97/EC 3 of the European Parliament and of the Council of 19 November 2008 and Council Directive 96/23/EC 4 of 29 April 1996, as amended by Council Regulation (EC) No. 806/2003 5 of 14 April 2003, Regulation (EC) No. 882/2004 6 of the European Parliament and of the Council of 29 April 2004 and Council Directive 2006/104/EC 7 of 20 November 2006, hereby make the following Regulations:

Citation

1.

1.

These Regulations may be cited as the European Communities (Control of Animal Remedies and their Residues) Regulations, 2009.

Interpretation

2.

2.

(1) In these Regulations—

“Act” means the Animal Remedies Act, 1993 (No. 23 of 1993);

“animal” has the same meaning as it has in Section 2 of the Act and in the Animal Remedies Act (Section 2) Order 2005 ( S.I. No. 733 of 2005 );

“approved laboratory” means a laboratory designated as an approved laboratory in accordance with Regulation 13;

“authorised officer” means a person who is an authorised officer within the meaning of the Act;

“Council Directives” means Council Directive 96/22/EC of 29 April 1996 and Council Directive 96/23/EC of 29 April 1996, as amended;

“eartag” means an approved eartag within the meaning of the European Communities (Identification of Bovines) Regulations 2009 ( S.I. No. 77 of 2009 );

“establishment” means an establishment approved or requiring to be approved under the European Communities (Food and Feed Hygiene) Regulations 2005 ( S.I. No. 910 of 2005 );

“farm animal” means a domestic animal of the bovine, porcine, ovine, caprine or cervine species, a domestic soliped, poultry, or rabbit, including a wild animal of those species;

“identity card” means—

“maximum residue limit” has the same meaning as it has in Council Regulation (EEC) No. 2377/90 8 of 26 June 1990;

“national reference laboratory” means a laboratory designated as a national reference laboratory in accordance with Regulation 13;

“official mark” means a mark in the form set out in the Schedule;

“prohibited animal remedy” means an animal remedy or ingredient for an animal remedy in respect of which, by virtue of these Regulations or the European Communities (Animal Remedies) (No. 2) Regulations (S.I. No. 786/2007), a licence, authorisation, registration or direction is required for the purpose of its administration to an animal or for other purposes and either—

“registered veterinary practitioner” means a veterinary practitioner registered under the Veterinary Practice Act 2005 (No. 22 of 2005);

“slaughter”, in relation to an animal, means slaughter for the purposes of the production of meat or other food intended for human or animal consumption.

Restriction on import, manufacture, sale or supply of certain animal remedies

3.

3.

(1) Subject to these Regulations, a person shall not manufacture, import, possess, sell or supply an animal remedy consisting of or containing—

Prohibition on administration of stilbenes or oestradiol 17 to a farm or aquaculture animal

4.

4.

(1) A person shall not administer, or cause to be administered to a farm or aquaculture animal, an animal remedy consisting of or containing—

Restriction on administration of certain substances to a farm or aquaculture animal.

5.

5.

(1) A person shall not administer, or cause to be administered to a farm or aquaculture animal, an animal remedy consisting of or containing a substance to which Regulation 3 (1) (b) or (c) applies, unless the administration is carried out in accordance with Regulation 8, 9 or 10.

Unlawful to sell or slaughter certain Animals, etc.

6.

6.

(1) A person shall not sell or slaughter a farm or aquaculture animal to which a prohibited animal remedy has been administered.

Detention of certain animals at establishments

7.

7.

(1) If an authorised officer has reasonable grounds for believing that a prohibited animal remedy has been administered to an animal presented for slaughter he or she shall—

until such time as the authorised officer is satisfied that the quantity of the authorised animal remedy present in the animal no longer exceeds the maximum residue limit.

Administration of certain animal remedies for the purposes of therapeutic treatment

8.

8.

(1) A registered veterinary practitioner may, for therapeutic purposes and in accordance with the terms and conditions of an animal remedies authorisation, administer an animal remedy, consisting of or containing testosterone, progesterone or derivatives thereof that readily yield the parent compound on hydrolysis after absorption at the site of application, to a farm animal,—

Administration of beta-agonists for the purposes of therapeutic treatment.

9.

9.

(1) A registered veterinary practitioner may, for the purpose of inducing tocolysis and in accordance with the terms and conditions of an animal remedies authorisation, administer, by injection, an animal remedy, consisting of or containing a beta-agonist, to a cow when calving.

Administration of certain animal remedies for zootechnical purposes

10.

10.

(1) A registered veterinary practitioner or, pursuant to a veterinary prescription, a person other than a registered veterinary practitioner, may, in accordance with the terms and conditions of an animal remedies authorisation, administer an animal remedy consisting of or containing a substance having an oestrogenic (other than oestradiol 17 or its ester-like derivatives), androgenic or gestagenic action to a farm animal to synchronise oestrus or prepare donors and recipients for the implantation of embryos.

Register of animal remedies administered

11.

11.

(1) A registered veterinary practitioner, to whom Regulation 8, 9 or 10 applies, shall cause to be established and maintained a register of animal remedies administered under those Regulations by him or her or by another person pursuant to a veterinary prescription issued by the registered veterinary practitioner.

Prohibition on administration

12.

12.

Notwithstanding Regulations 8, 9 or 10, a person shall not administer, or cause to be administered, an animal remedy, to which any of those Regulations apply, to—

Laboratories

13.

13.

(1) The Minister may designate, by instrument in writing, a laboratory as an approved laboratory, and a person for the time being employed or engaged in the analysis of specimens at a laboratory so designated may perform the functions of an approved laboratory.

Restriction of movement of certain animals

14.

14.

(1) If—

the authorised officer may give a direction, in accordance with paragraph (2), to—

or

from the land or premises or any part thereof as is specified in the direction,

Testing of animals

15.

15.

(1) If an authorised officer receives notification in writing from an approved laboratory or a national reference laboratory that, on analysis at the laboratory concerned, a specimen taken by him or her from an animal was found to contain a prohibited animal remedy, an authorised officer may, in accordance with Article 17 of Council Directive 96/23/EC of 29 April 1996, take specimens from a statistically representative sample of the batch of animals to which the said animal belongs.

Surrender of Identity Cards

16.

16.

(1) A person having in his or her possession, or under his or her control—

shall surrender the identity card to an authorised officer.

Marking of animals

17.

17.

(1) If an authorised officer receives notification in writing from an approved laboratory or a national reference laboratory that a specimen taken from an animal was found, on analysis at the laboratory concerned, to contain a prohibited animal remedy, the official mark in indelible form shall be affixed to the animal, from which the specimen was taken, in such manner as an authorised officer considers appropriate.

the official mark (other than in indelible form) shall be affixed to the animal concerned in such manner as an authorised officer considers appropriate.

Destruction of Animal where Illegal Treatment established

18.

18.

(1) If the official mark has been applied to an animal pursuant to Regulation 17 or if an authorised officer receives notification in writing from an approved laboratory or a national reference laboratory that a specimen taken from an animal was found, on analysis at the laboratory concerned, to contain a prohibited animal remedy, the authorised officer may destroy or cause to be destroyed the animal concerned and its carcase in such manner as he or she deems appropriate.

Unlawful to sell etc. an animal or animal product until certain conditions are met.

19.

19.

(1) A person shall not—

unless,

before the end of the withdrawal period,

Register of Certain Substances etc

20.

20.

(1) A person who engages in—

shall establish and maintain a register containing the particulars specified in paragraph (2).

Self Monitoring

21.

21.

(1) The owner or person in charge of an approved establishment shall, not later than the 31st day of October in each year, prepare and submit to the Minister a plan, in respect of the following year, for the detection of substances, veterinary drugs and contaminants specified in Annex 1 to Council Directive 96/23/EC of 29 April 1996 in—

at the establishment, and the plan shall, if approved by the Minister, be carried out by the owner or person in charge of the establishment in accordance with its terms.

the plan concerned, it, for the purposes of this Regulation, is deemed to have been approved by him or her.

Evidence by certificate in proceedings for an offence

22.

22.

(1) In proceedings for an offence consisting of a contravention of these Regulations, a certificate purporting to be signed by a person employed at an approved laboratory or a national reference laboratory, stating the capacity in which that person is so employed and stating any one or more of the following, namely—

shall, unless the contrary is proved, be evidence of the matters stated in the certificate.

Forgery of Documents

23.

23.

(1) A person shall not forge or utter knowing it to be forged—

Service of Documents

24.

24.

A direction or other document under these Regulations shall be addressed to the person concerned by name and may be served on or given to the person in one of the following ways—

Evidential Burden

25.

25.

In proceedings for an offence consisting of a contravention of these Regulations, it is not necessary to negative by evidence the existence of a marketing authorisation granted under Regulation (EC) No. 726/2004 and accordingly the onus of proving the grant or issue of such authorisation is on the defendant.

Persons not entitled to Community aid

26.

26.

(1) If the owner or person for the time being in charge of an establishment is convicted of an offence consisting of a contravention of Regulation 21(8), (9)(e), (f) or (g), or (11), or 23, or section 16 of the Act,—

is not entitled to receive Community aid for a period of 12 months commencing on the date of such conviction.

Implied condition in contract of sale

27.

27.

(1) In every contract of sale there shall be an implied condition on the part of the seller that all reasonable precautions have been taken and all due diligence has been exercised to ensure—

other than in accordance with these Regulations.

but only if the express term is fair and reasonable and has been specifically brought to the attention of the buyer.

Inspection by authorised officers, etc.

28.

28.

(1) If an authorised officer or member of the Garda Síochána or an officer of Customs and Excise has reasonable cause to suspect that—

the authorised officer or member of the Garda Síochána or officer of Customs and Excise (in this section referred to as “the relevant person”) may, subject to paragraph (2), stop any such vehicle or enter (if necessary by force) any such land or premises, or land or premises used in connection with such land or premises, or any such vehicle, and there, or at any other place, and with such authorised officers, members of the Garda Síochána and officers of Customs and Excise (if any) as the relevant person considers appropriate—

in accordance with these Regulations,

Search warrant

29.

29.

(1) If a judge of the District Court is satisfied by information on oath of an authorised officer, member of the Garda Síochána or an officer of Customs and Excise that there is reasonable cause for suspecting that—

the judge may issue a search warrant under this Regulation.

Search of suspects, etc.

30.

30.

(1) If, with reasonable cause, a member of the Garda Síochána or an officer of Customs and Excise suspects that a person is in possession in contravention of these Regulations of an animal remedy or an ingredient for an animal remedy, the member or officer may without warrant—

Power of arrest.

31.

31.

(1) Where, with reasonable cause, a member of the Garda Síochána suspects that—

he or she may arrest the person without warrant.

he or she may arrest the person without warrant if—

Obstruction

32.

32.

A person shall not obstruct or impede an authorised officer, member of the Garda Síochána or officer of Customs and Excise in the due exercise of any of the functions conferred or exercisable by the authorised officer, member of the Garda Síochána or officer of Customs and Excise under these Regulations.

Impersonation of authorised officer, etc.

33.

33.

(1) A person shall not, with the intention to deceive—

a person duly appointed as an authorised person, officer, inspector, examiner or other officer of the Minister or a person otherwise duly appointed by or with the authority of the Minister or of any other purported member of the Government exercising any functions of the Minister either—

duly issued for the purpose of identifying the person in possession of the document as a person duly authorised by, or a duly authorised officer, inspector, examiner or other officer of, the Minister or otherwise duly appointed by or with the authority of the Minister or, in the case of sub-paragraph (b) or (c), of any other purported member of the Government exercising any functions of the Minister either—

Offences and penalties

34.

34.

(1) A person who—

commits an offence.

Revocation and Saver

35.

35.

(1) The European Communities (Control of Animal Remedies and their Residues) Regulations 2007 ( S.I. No. 143 of 2007 ) are revoked.

SCHEDULE Official Mark

GIVEN under my Official Seal,

7 May 2009

BRENDAN SMITH.

Minister for Agriculture, Fisheries and Food.

EXPLANATORY NOTE

(This Note is not part of the Instrument and does not purport to be a legal interpretation.)

These Regulations implement in the State the provisions of Council Directive 96/22/EC of 29 April 1996 containing the prohibition in stockfarming of certain substances having hormonal or thyrostatic action and of beta agonists and Council Directive 96/23 of 29 April 1996 on measures to monitor certain substances and residues thereof in live animals and animal products.

Footnotes

1

O.J. L 125 of 23.5.96

2

O.J. L 262 of 14.10.2003

3

O.J. L 318 of 28.11.2008

4

O.J. L 125 of 23.5.96

5

O.J. L 122 of 15.5.2003

6

O.J. L 191 of 28.5.2004

7

OJ. L 363 of 20.12.2006

8

OJ L 224. 18.8.1990

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