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. )

Implementing Regulation (EU) 2018/84 · Regulation · 3 articles

Data as of 2026-07-04 · Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. · Read the official text ↗

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 .

Supplementary provisions

ANNEXSupplementary provisions

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’.

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Source: EUR-Lex (Publications Office of the EU), © European Union, reuse permitted under Commission Decision 2011/833/EU.

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