http://www.legislation.gov.uk/eur/2012/466Commission Implementing Regulation (EU) No 466/2012 of 1 June 2012 amending the Annex to Regulation (EU) No 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance clorsulon (Text with EEA relevance)Commission Implementing Regulation (EU) No 466/2012Commission Implementing Regulation (EU) No 466/2012 of 1 June 2012 amending the Annex to Regulation (EU) No 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance clorsulon (Text with EEA relevance)2020-12-11King's Printer of Acts of Parliamenthttps://webarchive.nationalarchives.gov.uk/eu-exit/https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:32012R0466texttext/xmlen2012-06-01

Commission Implementing Regulation (EU) No 466/2012

of 1 June 2012

amending the Annex to Regulation (EU) No 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance clorsulon

(Text with EEA relevance)

THE EUROPEAN COMMISSION,

Having regard to the Treaty on the Functioning of the European Union,

Having regard to Regulation (EC) No 470/2009 of the European Parliament and of the Council of 6 May 2009 laying down Community procedures for the establishment of residue limits of pharmacologically active substances in foodstuffs of animal origin, repealing Council Regulation (EEC) No 2377/90 and amending Directive 2001/82/EC of the European Parliament and of the Council and Regulation (EC) No 726/2004 of the European Parliament and the Council

OJ L 152, 16.6.2009, p. 11.

, and in particular Article 14 in conjunction with Article 17 thereof,

Having regard to the opinion of the European Medicines Agency formulated by the Committee for Medicinal Products for Veterinary Use,

Whereas:

(1)

The maximum residue limit (MRL) for pharmacologically active substances intended for use in the Union in veterinary medicinal products for food-producing animals or in biocidal products used in animal husbandry should be established in accordance with Regulation (EC) No 470/2009.

(2)

Pharmacologically active substances and their classification regarding MRLs in foodstuffs of animal origin are set out in the Annex to Commission Regulation (EU) No 37/2010 of 22 December 2009 on pharmacologically active substances and their classification regarding MRLs in foodstuffs of animal origin

OJ L 15, 20.1.2010, p. 1.

(3)

Clorsulon is currently included in Table 1 of the Annex to Regulation (EU) No 37/2010 as an allowed substance, for bovine species, applicable to muscle, liver and kidney, excluding animals producing milk for human consumption.

(4)

Ireland has submitted to the European Medicines Agency a request for an opinion for the extrapolation of the existing entry for clorsulon applicable to bovine milk.

(5)

The Committee for Medicinal Products for Veterinary Use (CVMP) has recommended the establishment of a provisional MRL for clorsulon for bovine milk and the removal of the provision banning the use of that substance in animals from which milk is produced for human consumption.

(6)

The entry for clorsulon in Table 1 of the Annex to Regulation (EU) No 37/2010 should therefore be amended to include the recommended provisional MRL for bovine milk and to remove the existing ban.

(7)

The provisional MRL for clorsulon set out in that Table should expire on 1 January 2014. The CVMP recommended a two-year period to allow for the completion of scientific studies required to respond to the list of questions addressed by the CVMP to Ireland.

(8)

It is appropriate to provide for a reasonable period of time for the stakeholders concerned to take measures that may be required to comply with the newly set MRL.

(9)

The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee on Veterinary Medicinal Products,

HAS ADOPTED THIS REGULATION:

Article 1

The Annex to Regulation (EU) No 37/2010 is amended as set out in the Annex to this Regulation.

Article 2

This Regulation shall enter into force on the third day following that of its publication in the Official Journal of the European Union.

It shall apply from 1 August 2012.

This Regulation shall be binding in its entirety and directly applicable in all Member States.

Done at Brussels, 1 June 2012.

For the Commission

The President

José Manuel Barroso

ANNEX

The entry corresponding to clorsulon in Table 1 of the Annex to Regulation (EU) No 37/2010 is replaced by the following:

Pharmacologically active substance
Marker residue
Animal species
MRL
Target tissues
Other provisions(according to Article 14(7) of Regulation (EC) No 470/2009)
Therapeutic classification
‘Clorsulon
Clorsulon
Bovine
35 μg/kg
Muscle
Antiparasitic agents/Agents against endoparasites’
100 μg/kg
Liver
200 μg/kg
Kidney
16 μg/kg
Milk
Provisional MRL shall expire on 1 January 2014

Pharmacologically active substance	Marker residue	Animal species	MRL	Target tissues	Other provisions(according to Article 14(7) of Regulation (EC) No 470/2009)	Therapeutic classification
‘Clorsulon	Clorsulon	Bovine	35 μg/kg	Muscle		Antiparasitic agents/Agents against endoparasites’
			100 μg/kg	Liver
			200 μg/kg	Kidney
			16 μg/kg	Milk	Provisional MRL shall expire on 1 January 2014