法律人 LawPlayer logo

資料由法律人 LawPlayer整理提供·EU law / curated by LawPlayer from EUR-Lex

Regulation

Commission Implementing Regulation (EU) 2015/1106 of 8 July 2015 amending Implementing Regulations (EU) No 540/2011 and (EU) No 1037/2012 as regards the conditions of approval of the active substance isopyrazam (Text with EEA relevance)

CELEX
Implementing Regulation (EU) 2015/1106
Date of document
Articles
3
Source
EUR-Lex
Article 1Amendments to Implementing Regulation (EU) No 540/2011

In the column ‘Specific provisions’ of row 27, isopyrazam, of Part B of the Annex to Implementing Regulation (EU) No 540/2011, the last paragraph is replaced by the following:

‘The applicant shall submit to the Commission, the Member States and the Authority this information by 31 July 2017.’

Article 2Amendments to Implementing Regulation (EU) No 1037/2012

In the column ‘Specific provisions’ of the Annex to Implementing Regulation (EU) No 1037/2012, the last paragraph is replaced by the following:

‘The applicant shall submit to the Commission, the Member States and the Authority this information by 31 July 2017.’

Article 3Entry into force

This Regulation shall enter into force on the day following that of its publication in the Official Journal of the European Union .

3 articles

Cite this act

Commission Implementing Regulation (EU) 2015/1106 of 8 July 2015 amending Implementing Regulations (EU) No 540/2011 and (EU) No 1037/2012 as regards the conditions of approval of the active substance isopyrazam (Text with EEA relevance) (EUR-Lex). Retrieved via LawPlayer, https://lawplayer.com/eu/act/32015R1106

© European Union, https://eur-lex.europa.eu, 1998-2026. Reuse authorised under Commission Decision 2011/833/EU, provided the source is acknowledged.

EU-EurLex-Reuse-2011-833

本頁資料來源:EUR-Lex·整理提供:法律人 LawPlayer· lawplayer.com