Commission Implementing Regulation (EU) 2018/84 of 19 January 2018 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances chlorpyrifos, chlorpyrifos-methyl, clothianidin, copper compounds, dimoxystrobin, mancozeb, mecoprop-p, metiram, oxamyl, pethoxamid, propiconazole, propineb, propyzamide, pyraclostrobin and zoxamide (Text with EEA relevance)
Grade B
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Address https://gelex.eu/eli/EU/regulation/2018/84@2018-01-19/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 first paragraph of Article 17 thereof,
Whereas:
(1) Part A of the Annex to Commission Implementing Regulation (EU) No 540/2011 sets out the active substances deemed to have been approved under Regulation (EC) No 1107/2009.
(2) The approval periods of the active substances mecoprop-p, propiconazole, propineb, propyzamide, pyraclostrobin and zoxamide were last extended by Commission Implementing Regulation (EU) 2016/2016. The approval periods of those substances will expire on 31 January 2018.
(3) The approval periods of the active substances chlorpyrifos, chlorpyrifos-methyl, mancozeb and metiram were extended by Commission Implementing Regulation (EU) No 762/2013. The approval periods of those substances will expire on 31 January 2018.
(4) The approval periods of the active substances clothianidin, dimoxystrobin, oxamyl and pethoxamid were extended by Commission Implementing Regulation (EU) No 1136/2013. The approval periods of those substances will expire on 31 January 2018.
(5) The approval period of the active substance copper compounds was extended by Commission Implementing Regulation (EU) No 85/2014. The approval period of the substance will expire on 31 January 2018.
(6) Applications for the renewal of the approval of the substances referred to in recitals 2 to 5 were submitted in accordance with Commission Implementing Regulation (EU) No 844/2012.
(7) Due to the fact that the assessment of the substances has been delayed for reasons beyond the control of the applicants, the approvals of those active substances are likely to expire before a decision has been taken on their renewal. It is therefore necessary to extend their approval periods.
(8) In view of the aim of the first 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 the Annex to 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 entry into force of the Regulation providing that the approval of the active substance is not renewed, whichever date is later. As regards cases where the Commission will adopt a Regulation providing for the renewal of an active substance referred to in the Annex to this Regulation, the Commission will endeavour to set, as appropriate under the circumstances, the earliest possible application date.
(9) Taking into account that the approvals of the active substances expire on 31 January 2018, this Regulation should enter into force as soon as possible.
(10) Implementing Regulation (EU) No 540/2011 should therefore be amended accordingly.
(11) The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee on Plants, Animals, Food and Feed,
HAS ADOPTED THIS REGULATION:
Article 1
Part A of the Annex to Implementing Regulation (EU) No 540/2011 is amended in accordance with 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.
This Regulation shall be binding in its entirety and directly applicable in all Member States. Done at Brussels, 19 January 2018. For the Commission The President Jean-Claude Juncker
ANNEX
ANNEX
Part A of the Annex to Implementing Regulation (EU) No 540/2011 is amended as follows:
(1) in the sixth column, expiration of approval, of row 54, Propineb, the date is replaced by 31 January 2019;
(2) in the sixth column, expiration of approval, of row 55, Propyzamide, the date is replaced by 31 January 2019;
(3) in the sixth column, expiration of approval, of row 57, Mecoprop-P, the date is replaced by 31 January 2019;
(4) in the sixth column, expiration of approval, of row 58, Propiconazole, the date is replaced by 31 January 2019;
(5) in the sixth column, expiration of approval, of row 77, Zoxamide, the date is replaced by 31 January 2019;
(6) in the sixth column, expiration of approval, of row 81, Pyraclostrobin, the date is replaced by 31 January 2019;
(7) in the sixth column, expiration of approval, of row 111, Chlorpyrifos, the date is replaced by 31 January 2019;
(8) in the sixth column, expiration of approval, of row 112, Chlorpyrifos-methyl, the date is replaced by 31 January 2019;
(9) in the sixth column, expiration of approval, of row 114, Mancozeb, the date is replaced by 31 January 2019;
(10) in the sixth column, expiration of approval, of row 115, Metiram, the date is replaced by 31 January 2019;
(11) in the sixth column, expiration of approval, of row 116, Oxamyl, the date is replaced by 31 January 2019;
(12) in the sixth column, expiration of approval, of row 121, Clothianidin, the date is replaced by 31 January 2019;
(13) in the sixth column, expiration of approval, of row 122, Pethoxamid, the date is replaced by 31 January 2019;
(14) in the sixth column, expiration of approval, of row 128, Dimoxystrobin, the date is replaced by 31 January 2019;
(15) in the sixth column, expiration of approval, of row 277, Copper compounds, the date is replaced by 31 January 2019.
Versions
Cited by
- Commission Implementing Regulation (EU) 2018/309 of 1 March 2018 concerning the non-renewal of approval of the active substance propineb, 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) Regulation · Grade B
Commission Implementing Regulation (EU) 2018/84 extended the expiry date of propineb to 31 January 2019 in order to allow the renewal process to be completed before the expiry of the approval of that substance. However, given that a decision has been taken ahead of that extended expiry date, this Regulation should apply as soon as possible.
- Commission Implementing Regulation (EU) 2018/1796 of 20 November 2018 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances amidosulfuron, bifenox, chlorpyrifos, chlorpyrifos-methyl, clofentezine, dicamba, difenoconazole, diflubenzuron, diflufenican, dimoxystrobin, fenoxaprop-p, fenpropidin, lenacil, mancozeb, mecoprop-p, metiram, nicosulfuron, oxamyl, picloram, pyraclostrobin, pyriproxyfen and tritosulfuron (Text with EEA relevance) Regulation · Grade B
The approval periods of the active substances chlorpyrifos, chlorpyrifos-methyl, dimoxystrobin, mancozeb, mecoprop-p, metiram, oxamyl and pyraclostrobin were last extended by Commission Implementing Regulation (EU) 2018/84. The approval periods of those substances will expire on 31 January 2019.
- Commission Implementing Regulation (EU) 2018/1981 of 13 December 2018 renewing the approval of the active substances copper compounds, as candidates for substitution, 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) Regulation · Grade B
Commission Implementing Regulation (EU) 2018/84 extended the approval period of copper compounds to 31 January 2019 in order to allow the renewal process to be completed before the expiry of the approval of these substances. However, given that a decision on renewal has been taken ahead of this extended expiry date, this Regulation should apply from 1 January 2019.
- Commission Implementing Regulation (EU) 2018/692 of 7 May 2018 renewing the approval of the active substance zoxamide 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) Regulation · Grade B
Commission Implementing Regulation (EU) 2018/84 extended the expiry date of zoxamide to 31 January 2019 in order to allow the renewal process to be completed before the expiry of the approval of that active substance. However, given that a decision on renewal has been taken ahead of that extended expiry date, this Regulation should apply from 1 July 2018.
- Commission Implementing Regulation (EU) 2018/1865 of 28 November 2018 concerning the non-renewal of approval of the active substance propiconazole, 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 Commission Implementing Regulation (EU) No 540/2011 (Text with EEA relevance) Regulation · Grade B
Commission Implementing Regulation (EU) 2018/84 extended the expiry date of propiconazole to 31 January 2019 in order to allow the renewal process to be completed before the expiry of the approval period of that substance. Given that a decision is taken ahead of this extended expiry date, this Regulation should apply as soon as possible.
- Commission Implementing Regulation (EU) 2018/755 of 23 May 2018 renewing the approval of the active substance propyzamide, as a candidate for substitution, 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) Regulation · Grade B
Commission Implementing Regulation (EU) 2018/84 extended the approval period of propyzamide to 31 January 2019 in order to allow the renewal process to be completed before the expiry of the approval of that substance. However, given that a decision on renewal has been taken ahead of this extended expiry date, this Regulation should apply from 1 July 2018.
- Commission Implementing Regulation (EU) 2018/1264 of 20 September 2018 renewing the approval of the active substance pethoxamid 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) Regulation · Grade B
Commission Implementing Regulation (EU) 2018/84 extended the expiry date of pethoxamid to 31 January 2019 in order to allow the renewal process to be completed before the expiry of the approval of that active substance. However, given that a decision on renewal has been taken ahead of that extended expiry date, this Regulation should apply from 1 December 2018.
- P9_TA(2019)0099 Active substances, including dimoxystrobin and mancozeb European Parliament resolution of 18 December 2019 on the draft Commission implementing regulation amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances benfluralin, dimoxystrobin, fluazinam, flutolanil, mancozeb, mecoprop-P, mepiquat, metiram, oxamyl and pyraclostrobin (D064213/02 — 2019/2925(RSP)) 2021/C 255/01 Notice · Grade B
whereas the approval period of the active substance dimoxystrobin, which was originally due to have ended on 30 September 2016, has already been extended by 16 months by Commission Implementing Regulation (EU) No 1136/2013, followed by a one-year extension by Commission Implementing Regulation (EU) 2018/84, then another one-year extension by Commission Implementing Regulation (EU) 2018/1796, and is now again to be extended by one year by means of this draft Commission implementing regulation, which would extend the approval period to 31 January 2021;
- P9_TA(2019)0099 Active substances, including dimoxystrobin and mancozeb European Parliament resolution of 18 December 2019 on the draft Commission implementing regulation amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances benfluralin, dimoxystrobin, fluazinam, flutolanil, mancozeb, mecoprop-P, mepiquat, metiram, oxamyl and pyraclostrobin (D064213/02 — 2019/2925(RSP)) 2021/C 255/01 Notice · Grade B
whereas the approval period of the active substance mancozeb, which was originally due to have ended on 30 June 2016, has already been extended by 19 months by Commission Implementing Regulation (EU) No 762/2013, followed by a one-year extension by Implementing Regulation (EU) 2018/84, then another one-year extension by Implementing Regulation (EU) 2018/1796, and is now again to be extended by one year by means of this draft Commission implementing regulation, which would extend the approval period to 31 January 2021;