This document is an excerpt from the EUR-Lex website
Document 32016R0183
Commission Implementing Regulation (EU) 2016/183 of 11 February 2016 amending Implementing Regulation (EU) No 686/2012 allocating to Member States, for the purposes of the renewal procedure, the evaluation of the active substances whose approval expires by 31 December 2018 at the latest (Text with EEA relevance)
Commission Implementing Regulation (EU) 2016/183 of 11 February 2016 amending Implementing Regulation (EU) No 686/2012 allocating to Member States, for the purposes of the renewal procedure, the evaluation of the active substances whose approval expires by 31 December 2018 at the latest (Text with EEA relevance)
Commission Implementing Regulation (EU) 2016/183 of 11 February 2016 amending Implementing Regulation (EU) No 686/2012 allocating to Member States, for the purposes of the renewal procedure, the evaluation of the active substances whose approval expires by 31 December 2018 at the latest (Text with EEA relevance)
OJ L 37, 12.2.2016, p. 44–55
(BG, ES, CS, DA, DE, ET, EL, EN, FR, HR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)
In force
|
12.2.2016 |
EN |
Official Journal of the European Union |
L 37/44 |
COMMISSION IMPLEMENTING REGULATION (EU) 2016/183
of 11 February 2016
amending Implementing Regulation (EU) No 686/2012 allocating to Member States, for the purposes of the renewal procedure, the evaluation of the active substances whose approval expires by 31 December 2018 at the latest
(Text with EEA relevance)
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 (1), and in particular Article 19, thereof,
Whereas:
|
(1) |
Commission Implementing Regulation (EU) No 686/2012 (2) allocates, for the purposes of the renewal procedures, the evaluation of active substances whose approval expires by 31 December 2018 at the latest to the Member States, naming for each active substance a rapporteur and a co-rapporteur. It is appropriate to allocate the evaluation of active substances whose approval expires by 31 December 2021 at the latest. |
|
(2) |
That allocation should be made in such a way that a balance is achieved as regards the distribution of the responsibilities and the work between Member States. |
|
(3) |
Implementing Regulation (EU) No 686/2012 should therefore be amended accordingly. |
|
(4) |
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
Implementing Regulation (EU) No 686/2012 is amended as follows:
|
(1) |
The title is replaced by the following: ‘Commission Implementing Regulation (EU) No 686/2012 of 26 July 2012 allocating to Member States, for the purposes of the renewal procedure, the evaluation of active substances’. |
|
(2) |
The Annex to Implementing Regulation (EU) No 686/2012 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.
This Regulation shall be binding in its entirety and directly applicable in all Member States.
Done at Brussels, 11 February 2016.
For the Commission
The President
Jean-Claude JUNCKER
(1) OJ L 309, 24.11.2009, p. 1.
(2) Commission Implementing Regulation (EU) No 686/2012 of 26 July 2012 allocating to Member States, for the purposes of the renewal procedure, the evaluation of the active substances whose approval expires by 31 December 2018 at the latest (OJ L 200, 27.7.2012. p. 5).
ANNEX
The Annex to Implementing Regulation (EU) No 686/2012 is amended as follows:
|
(1) |
The word ‘ANNEX’ is replaced by the following: ‘ANNEX PART A Allocation of the evaluation of active substances whose approval expires by 31 December 2018 at the latest’ |
|
(2) |
The following Part B is added: ‘PART B Allocation of the evaluation of active substances whose approval expires after 31 December 2018 and not later than 31 December 2021
|