Commission Regulation (EU) No 823/2012 of 14 September 2012 derogating from Implementing Regulation (EU) No 540/2011 as regards the expiry dates of the approval of the active substances 2,4-DB, benzoic acid, beta-cyfluthrin, carfentrazone ethyl, Coniothyrium minitans Strain CON/M/91-08 (DSM 9660), cyazofamid, cyfluthrin, deltamethrin, dimethenamid-P, ethofumesate, ethoxysulfuron, fenamidone, flazasulfuron, flufenacet, flurtamone, foramsulfuron, fosthiazate, imazamox, iodosulfuron, iprodione, isoxaflutole, linuron, maleic hydrazide, mecoprop, mecoprop-P, mesosulfuron, mesotrione, oxadiargyl, oxasulfuron, pendimethalin, picoxystrobin, propiconazole, propineb, propoxycarbazone, propyzamide, pyraclostrobin, silthiofam, trifloxystrobin, warfarin and zoxamide (Text with EEA relevance)
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Address https://gelex.eu/eli/EU/regulation/2012/823@2012-09-14/en
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, and in particular the second paragraph of Article 17 thereof,
Whereas:
(1) For active substances set out in Part A of the Annex to 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 for which approvals expire before 14 June 2014, applicants could not give the three years’ notice required under Article 15(1) of Regulation (EC) No 1107/2009 as regards applications for renewal.
(2) Therefore, it is necessary to extend the period of approval of those active substances taking into account, the elements provided for in the third paragraph of Article 17 of Regulation (EC) No 1107/2009.
(3) In view of the aim of the second paragraph of Article 17 of Regulation (EC) No 1107/2009, as regards cases where no application is submitted three years before the respective expiry date laid down in Article 1 of this Regulation, the Commission will set the expiry date at the same date as before this Regulation or at the earliest date thereafter.
(4) In view of the aim of the second paragraph of Article 17 of Regulation (EC) No 1107/2009, as regards cases where the Commission will adopt a Regulation providing that the approval of an active substance referred to in Article 1 of this Regulation is not renewed because the approval criteria are not satisfied, the Commission will set the expiry date at the same date as before this Regulation or at the date of the adoption of the Regulation providing that the approval of the active substance is not renewed, whichever date is later.
(5) The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee on the Food Chain and Animal Health and neither the European Parliament nor the Council has opposed them,
HAS ADOPTED THIS REGULATION:
Article 1 Expiry dates
By way of derogation from Part A of the Annex to Implementing Regulation (EU) No 540/2011, the following expiry dates shall apply:
(1) 31 July 2016, as regards the active substances: ethofumesate (entry 29), imazamox (entry 41), oxasulfuron (entry 42), ethoxysulfuron (entry 43), foramsulfuron (entry 44), oxadiargyl (entry 45), cyazofamid (entry 46), linuron (entry 51), pendimethalin (entry 53), trifloxystrobin (entry 59), carfentrazone ethyl (entry 60), mesotrione (entry 61), fenamidone (entry 62), isoxaflutole (entry 63) and warfarin (entry 120);
(2) 31 October 2016, as regards the active substances: deltamethrin (entry 40), 2,4-DB (entry 47), beta-cyfluthrin (entry 48), cyfluthrin (entry 49), iprodione (entry 50), maleic hydrazide (entry 52), flurtamone (entry 64), flufenacet (entry 65), iodosulfuron (entry 66), dimethenamid-P (entry 67), picoxystrobin (entry 68), fosthiazate (entry 69), silthiofam (entry 70) and Coniothyrium minitans Strain CON/M/91-08 (DSM 9660) (entry 71);
(3) 31 January 2017, as regards the active substances: propineb (entry 54), propyzamide (entry 55), mecoprop (entry 56), mecoprop-P (entry 57), propiconazole (entry 58), mesosulfuron (entry 75), propoxycarbazone (entry 76), zoxamide (entry 77), benzoic acid (entry 79), flazasulfuron (entry 80) and pyraclostrobin (entry 81).
Article 2 Entry into force
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, 14 September 2012. For the Commission The President José Manuel Barroso
Versions
Cited by
- Commission Implementing Regulation (EU) 2016/950 of 15 June 2016 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances 2,4-DB, beta-cyfluthrin, carfentrazone ethyl, Coniothyrium minitans Strain CON/M/91-08 (DSM 9660), cyazofamid, deltamethrin, dimethenamid-P, ethofumesate, fenamidone, flufenacet, flurtamone, foramsulfuron, fosthiazate, imazamox, iodosulfuron, iprodione, isoxaflutole, linuron, maleic hydrazide, mesotrione, oxasulfuron, pendimethalin, picoxystrobin, silthiofam and trifloxystrobin (Text with EEA relevance) Regulation · Grade B
The approval periods of the active substances carfentrazone ethyl, cyazofamid, ethofumesate, fenamidone, foramsulfuron, imazamox, isoxaflutole, linuron, mesotrione, oxasulfuron, pendimethalin and trifloxystrobin were derogated from by Commission Regulation (EU) No 823/2012. The approval of those substances will expire on 31 July 2016.
- Commission Implementing Regulation (EU) 2016/950 of 15 June 2016 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances 2,4-DB, beta-cyfluthrin, carfentrazone ethyl, Coniothyrium minitans Strain CON/M/91-08 (DSM 9660), cyazofamid, deltamethrin, dimethenamid-P, ethofumesate, fenamidone, flufenacet, flurtamone, foramsulfuron, fosthiazate, imazamox, iodosulfuron, iprodione, isoxaflutole, linuron, maleic hydrazide, mesotrione, oxasulfuron, pendimethalin, picoxystrobin, silthiofam and trifloxystrobin (Text with EEA relevance) Regulation · Grade B
The approval periods of the active substances 2,4-DB, beta-cyfluthrin, Coniothyrium minitans Strain CON/M/91-08 (DSM 9660), deltamethrin, dimethenamid-P, flufenacet, flurtamone, fosthiazate, iodosulfuron, iprodione, maleic hydrazide, picoxystrobin and silthiofam were derogated from by Regulation (EU) No 823/2012. The approval of these substances will expire on 31 October 2016.
- Commission Implementing Regulation (EU) 2016/2016 of 17 November 2016 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances acetamiprid, benzoic acid, flazasulfuron, mecoprop-P, mepanipyrim, mesosulfuron, propineb, propoxycarbazon, propyzamide, propiconazole, Pseudomonas chlororaphis Strain: MA 342, pyraclostrobin, quinoxyfen, thiacloprid, thiram, ziram, zoxamide (Text with EEA relevance) Regulation · Grade B
The approval periods of the active substances benzoic acid, flazasulfuron, mecoprop-P, mesosulfuron, propineb, propoxycarbazon, propyzamide, propiconazole, pyraclostrobin, and zoxamide were derogated from by Commission Regulation (EU) No 823/2012. The approval of those substances will expire on 31 January 2017.
- Commission Regulation (EU) No 186/2014 of 26 February 2014 amending Regulation (EU) No 823/2012 as regards the expiry dates of the approval of the active substances ethoxysulfuron, oxadiargyl and warfarin (Text with EEA relevance) Regulation · Grade B
For the active substances ethoxysulfuron, oxadiargyl and warfarin, Commission Regulation (EU) No 823/2012 postponed the expiry of the approval period, as set out in Commission Implementing Regulation (EU) No 540/2011 to 31 July 2016 in order to enable applicants to give the three years’ notice required under Article 15(1) of Regulation (EC) No 1107/2009.
- Commission Regulation (EU) No 186/2014 of 26 February 2014 amending Regulation (EU) No 823/2012 as regards the expiry dates of the approval of the active substances ethoxysulfuron, oxadiargyl and warfarin (Text with EEA relevance) Regulation · Grade B
Since no such applications were submitted it is appropriate to set the expiry date at the earliest date possible after the original date of expiry as set before the adoption of Regulation (EU) No 823/2012.
- Commission Regulation (EU) No 186/2014 of 26 February 2014 amending Regulation (EU) No 823/2012 as regards the expiry dates of the approval of the active substances ethoxysulfuron, oxadiargyl and warfarin (Text with EEA relevance) Regulation · Grade B
Regulation (EU) No 823/2012 should therefore be amended accordingly.
- Commission Regulation (EU) 2015/1040 of 30 June 2015 amending Annexes II, III and V to Regulation (EC) No 396/2005 of the European Parliament and of the Council as regards maximum residue levels for azoxystrobin, dimoxystrobin, fluroxypyr, methoxyfenozide, metrafenone, oxadiargyl and tribenuron in or on certain products (Text with EEA relevance) Regulation · Grade B
Pursuant to Commission Regulation (EU) No 823/2012 the approval of oxadiargyl expired on 31 March 2014. All existing authorisations for plant protection products containing the active substance oxadiargyl have been revoked and grace periods end on 30 September 2015 at the latest. In accordance with Article 17 of Regulation (EC) No 396/2005 in conjunction with Article 14(1) thereof the MRLs set out for that active substance in Annexes II and III should therefore be deleted. This should not apply to those MRLs corresponding to CXLs based on uses in third countries provided that they are acceptab
- Commission Regulation (EU) No 460/2014 of 5 May 2014 amending Regulation (EU) No 823/2012 as regards the expiry date of the approval of the active substance cyfluthrin (Text with EEA relevance) Regulation · Grade B
For the active substance cyfluthrin, Commission Regulation (EU) No 823/2012 postponed the expiry of the approval period, as set out in Commission Implementing Regulation (EU) No 540/2011 to 31 October 2016 in order to enable applicants to give the three years' notice required under Article 15(1) of Regulation (EC) No 1107/2009.
- Commission Regulation (EU) No 460/2014 of 5 May 2014 amending Regulation (EU) No 823/2012 as regards the expiry date of the approval of the active substance cyfluthrin (Text with EEA relevance) Regulation · Grade B
Since no such application was submitted it is appropriate to set the expiry date at the earliest date possible after the original date of expiry as set before the adoption of Regulation (EU) No 823/2012.
- Commission Regulation (EU) No 460/2014 of 5 May 2014 amending Regulation (EU) No 823/2012 as regards the expiry date of the approval of the active substance cyfluthrin (Text with EEA relevance) Regulation · Grade B
Regulation (EU) No 823/2012 should therefore be amended accordingly.