Commission Implementing Regulation (EU) 2017/1511 of 30 August 2017 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances 1-methylcyclopropene, beta-cyfluthrin, chlorothalonil, chlorotoluron, cypermethrin, daminozide, deltamethrin, dimethenamid-p, flufenacet, flurtamone, forchlorfenuron, fosthiazate, indoxacarb, iprodione, MCPA, MCPB, silthiofam, thiophanate-methyl and tribenuron (Text with EEA relevance. )

Implementing Regulation (EU) 2017/1511 · 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 twentieth 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 40, Deltamethrin, the date is replaced by ‘31 October 2018’; (2) in the sixth column, expiration of approval, of row 48, Beta-cyfluthrin, the date is replaced by ‘31 October 2018’; (3) in the sixth column, expiration of approval, of row 50, Iprodione, the date is replaced by ‘31 October 2018’; (4) in the sixth column, expiration of approval, of row 64, Flurtamone, the date is replaced by ‘31 October 2018’; (5) in the sixth column, expiration of approval, of row 65, Flufenacet, the date is replaced by ‘31 October 2018’; (6) in the sixth column, expiration of approval, of row 67, Dimethenamid-P, the date is replaced by ‘31 October 2018’; (7) in the sixth column, expiration of approval, of row 69, Fosthiazate, the date is replaced by ‘31 October 2018’; (8) in the sixth column, expiration of approval, of row 70, Silthiofam, the date is replaced by ‘31 October 2018’; (9) in the sixth column, expiration of approval, of row 101, Chlorothalonil, the date is replaced by ‘31 October 2018’; (10) in the sixth column, expiration of approval, of row 102, Chlorotoluron, the date is replaced by ‘31 October 2018’; (11) in the sixth column, expiration of approval, of row 103, Cypermethrin, the date is replaced by ‘31 October 2018’; (12) in the sixth column, expiration of approval, of row 104, Daminozide, the date is replaced by ‘31 October 2018’; (13) in the sixth column, expiration of approval, of row 105, Thiophanate-methyl, the date is replaced by ‘31 October 2018’; (14) in the sixth column, expiration of approval, of row 106, Tribenuron, the date is replaced by ‘31 October 2018’; (15) in the sixth column, expiration of approval, of row 107, MCPA, the date is replaced by ‘31 October 2018’; (16) in the sixth column, expiration of approval, of row 108, MCPB, the date is replaced by ‘31 October 2018’; (17) in the sixth column, expiration of approval, of row 117, 1-methylcyclopropene, the date is replaced by ‘31 October 2018’; (18) in the sixth column, expiration of approval, of row 118, Forchlorfenuron, the date is replaced by ‘31 October 2018’; (19) in the sixth column, expiration of approval, of row 119, Indoxacarb, the date is replaced by ‘31 October 2018’.

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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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