Commission Implementing Regulation (EU) 2015/1192 of 20 July 2015 approving the active substance terpenoid blend QRD 460, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market, and amending the Annex to Commission Implementing Regulation (EU) No 540/2011 (Text with EEA relevance)

Type Implementing Regulation
Publication 2015-07-21
State In force
Text As published
Department European Commission
Source EUR-Lex
articles 3

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.

Reform history JSON API
21.7.2015 EN Official Journal of the European Union L 193/124

THE EUROPEAN COMMISSION,

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

Having regard to Regulation (EC) No 1107/2009 of the European Parliament and of the Council of 21 October 2009 concerning the placing of plant protection products on the market and repealing Council Directives 79/117/EEC and 91/414/EEC 1, and in particular Article 13(2) thereof,

Whereas:

HAS ADOPTED THIS REGULATION:

Article 1

Approval of active substance

The active substance terpenoid blend QRD 460, as specified in Annex I, is approved subject to the conditions laid down in that Annex.

Article 2

Amendments to Implementing Regulation (EU) No 540/2011

The Annex to Implementing Regulation (EU) No 540/2011 is amended in accordance with Annex II to this Regulation.

Article 3

Entry into force and date of application

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

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

Done at Brussels, 20 July 2015.

For the Commission

The President

Jean-Claude JUNCKER

2

EFSA Journal 2014;12(10):3816. Available online: www.efsa.europa.eu

3

Commission Implementing Regulation (EU) No 540/2011 of 25 May 2011 implementing Regulation (EC) No 1107/2009 of the European Parliament and of the Council as regards the list of approved active substances (OJ L 153, 11.6.2011, p. 1).

ANNEX I

Common Name, Identification Numbers IUPAC Name Purity4 Date of approval Expiration of approval Specific provisions
Terpenoid blend QRD 460 CIPAC No: 982 Terpenoid blend QRD 460 is a blend of three components: — α-terpinene: 1-isopropyl-4-methylcyclohexa-1,3-diene; — p-cymene: 1-isopropyl-4-methylbenzene; — d-limonene: (R)-4-isopropenyl-1-methylcyclohexene. The nominal concentration of each component in the active substance as manufactured should be as follows: — α-terpinene: 59,7 %; — p-cymene: 22,4 %; — d-limonene: 17,9 %. Each component should have a minimum purity as follows: — α-terpinene: 89 %; — p-cymene: 97 %; — d-limonene: 93 %. 10 August 2015 10 August 2025 For the implementation of the uniform principles as referred to in Article 29(6) of Regulation (EC) No 1107/2009, the conclusions of the review report on terpenoid blend QRD-460, and in particular Appendices I and II thereof, shall be taken into account. In this overall assessment Member States shall pay particular attention to: (a) the stability of formulations on storage; (b) the protection of operators and workers, ensuring that conditions of use include the application of adequate personal protective equipment, where appropriate; (c) the protection of groundwater, when the substance is applied in regions with vulnerable soil and/or climatic conditions; (d) the protection of surface water and aquatic organisms; (e) the protection of bees and non-target arthropods. Conditions of use shall include risk mitigation measures, where appropriate. The applicant shall submit confirmatory information as regards: (1) the technical specification of the active substance as manufactured (5 batch analysis for the blend should be provided), supported by acceptable and validated methods of analysis. It should be confirmed that there are no relevant impurities present in the technical material; (2) the equivalence of the material used in the toxicological and ecotoxicological studies with the confirmed technical specification. The applicant shall submit that information to the Commission, the Member States and the Authority by 10 February 2016.
4

Further details on identity and specification of active substance are provided in the review report.

ANNEX II

In Part B of the Annex to Implementing Regulation (EU) No 540/2011, the following entry is added:

Common Name, Identification Numbers IUPAC Name Purity5 Date of approval Expiration of approval Specific provisions
‘84 Terpenoid blend QRD 460 CIPAC No: 982 Terpenoid blend QRD 460 is a blend of three components: — α-terpinene: 1-isopropyl-4-methylcyclohexa-1,3-diene; — p-cymene: 1-isopropyl-4-methylbenzene; — d-limonene: (R)-4-isopropenyl-1-methylcyclohexene. The nominal concentration of each component in the active substance as manufactured should be as follows: — α-terpinene: 59,7 %; — p-cymene: 22,4 %; — d-limonene: 17,9 %. Each component should have a minimum purity as follows: — α-terpinene: 89 %; — p-cymene: 97 %; — d-limonene: 93 %. 10 August 2015 10 August 2025 For the implementation of the uniform principles as referred to in Article 29(6) of Regulation (EC) No 1107/2009, the conclusions of the review report on terpenoid blend QRD-460, and in particular Appendices I and II thereof, shall be taken into account. In this overall assessment Member States shall pay particular attention to: (a) the stability of formulations on storage; (b) the protection of operators and workers, ensuring that conditions of use include the application of adequate personal protective equipment, where appropriate; (c) the protection of groundwater, when the substance is applied in regions with vulnerable soil and/or climatic conditions; (d) the protection of surface water and aquatic organisms; (e) the protection of bees and non-target arthropods. Conditions of use shall include risk mitigation measures, where appropriate. The applicant shall submit confirmatory information as regards: (1) the technical specification of the active substance as manufactured (5 batch analysis for the blend should be provided), supported by acceptable and validated methods of analysis. It should be confirmed that there are no relevant impurities present in the technical material; (2) the equivalence of the material used in the toxicological and ecotoxicological studies with the confirmed technical specification. The applicant shall submit that information to the Commission, the Member States and the Authority by 10 February 2016.’
5

Further details on identity and specification of active substance are provided in the review report.

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