Article 1
The Annex to Implementing Regulation (EU) No 540/2011 is amended in accordance with the Annex to this Regulation.
Commission Implementing Regulation (EU) 2024/324 of 19 January 2024 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances benzovindiflupyr, bromuconazole, buprofezin, cyflufenamid, fluazinam, fluopyram, flutolanil, lambda-cyhalothrin, mecoprop-P, mepiquat, metsulfuron-methyl, phosphane and pyraclostrobin
Commission Implementing Regulation (EU) 2024/324 of 19 January 2024 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances benzovindiflupyr, bromuconazole, buprofezin, cyflufenamid, fluazinam, fluopyram, flutolanil, lambda-cyhalothrin, mecoprop-P, mepiquat, metsulfuron-methyl, phosphane and pyraclostrobin
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 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 The Annex to Implementing Regulation (EU) No 540/2011 is amended as follows: 1. Part A is amended as follows: (1) in the sixth column, expiration of approval, of row 57, Mecoprop-P, the date is replaced by ‘15 May 2025’; (2) in the sixth column, expiration of approval, of row 81, Pyraclostrobin, the date is replaced by ‘15 September 2025’; (3) in the sixth column, expiration of approval, of row 187, Flutolanil, the date is replaced by ‘15 June 2025’; (4) in the sixth column, expiration of approval, of row 189, Fluazinam, the date is replaced by ‘15 April 2026’; (5) in the sixth column, expiration of approval, of row 191, Mepiquat, the date is replaced by ‘15 October 2025’; (6) in the sixth column, expiration of approval, of row 296, Cyflufenamid, the date is replaced by ‘30 June 2027’; (7) in the sixth column, expiration of approval, of row 318, Bromuconazole, the date is replaced by ‘30 April 2027’; (8) in the sixth column, expiration of approval, of row 320, Buprofezin, the date is replaced by ‘15 December 2025’. 2. Part B is amended as follows: (1) in the sixth column, expiration of approval, of row 28, Phosphane, the date is replaced by ‘15 March 2026’; (2) in the sixth column, expiration of approval, of row 51, Fluopyram, the date is replaced by ‘30 June 2026’. 3. Part E is amended as follows: (1) in the sixth column, expiration of approval, of row 3, Metsulfuron-methyl, the date is replaced by ‘31 August 2026’; (2) in the sixth column, expiration of approval, of row 4, Benzovindiflupyr, the date is replaced by ‘2 August 2026’; (3) in the sixth column, expiration of approval, of row 5, Lambda-cyhalothrin, the date is replaced by ‘31 August 2026’.
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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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