
Article 1 
Annex I to Implementing Regulation (EU) No 788/2011 is amended in accordance with Annex I to this Regulation.
Article 2 
The Annex to Implementing Regulation (EU) No 540/2011 is amended in accordance with Annex II to this Regulation.
Article 3 
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, 8 March 2013.
For the Commission
The President
José Manuel BARROSO
ANNEX I

The column ‘Specific provisions’ in Annex I to Implementing Regulation (EU) No 788/2011 is replaced by the following:
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PART A Only uses as herbicide may be authorised.

PART B For the implementation of the uniform principles as referred to in Article 29(6) of Regulation (EC) No 1107/2009, the conclusions of the review report on fluazifop-P, and in particular Appendices I and II thereof, as finalised in the Standing Committee on the Food Chain and Animal Health on 1 February 2013, shall be taken into account.
In this overall assessment Member States shall:

— pay particular attention to consumer safety as regards the occurrence in groundwater of the metabolite compound X;
— pay particular attention to operator safety and shall ensure that conditions of use include the application of adequate personal protective equipment, where appropriate;
— pay particular attention to the protection of surface water and groundwater in vulnerable zones;
— pay particular attention to the risk for non-target plants.
Conditions of use shall include risk mitigation measures, where appropriate.
The applicant shall submit confirmatory information as regards:

((1)) the specification of the technical material, as commercially manufactured, including information on the relevance of the impurity R154719;
((2)) the equivalence between the specifications of the technical material, as commercially manufactured, and the specifications of the test material used in the toxicity studies;
((3)) the potential long-term risk to herbivorous mammals;
((4)) the fate and behaviour in the environment of the metabolite compounds X and IV;
((5)) the potential risk to fish and aquatic invertebrates for the metabolite compound IV.
The applicant shall submit to the Commission, the Member States and the Authority the information set out in points (1) and (2) by 30 June 2012 and the information set out in points (3), (4) and (5) by 31 December 2013.
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ANNEX II

The column ‘Specific provisions’ of row 15, fluazifop-P, of Part B of the Annex to Implementing Regulation (EU) No 540/2011 is replaced by the following:
'
PART A Only uses as herbicide may be authorised.

PART B For the implementation of the uniform principles as referred to in Article 29(6) of Regulation (EC) No 1107/2009, the conclusions of the review report on fluazifop-P, and in particular Appendices I and II thereof, as finalised in the Standing Committee on the Food Chain and Animal Health on 1 February 2013, shall be taken into account.
In this overall assessment Member States shall:

— pay particular attention to consumer safety as regards the occurrence in groundwater of the metabolite compound X;
— pay particular attention to operator safety and shall ensure that conditions of use include the application of adequate personal protective equipment, where appropriate;
— pay particular attention to the protection of surface water and groundwater in vulnerable zones;
— pay particular attention to the risk for non-target plants.
Conditions of use shall include risk mitigation measures, where appropriate.
The applicant shall submit confirmatory information as regards:

((1)) the specification of the technical material, as commercially manufactured, including information on the relevance of the impurity R154719;
((2)) the equivalence between the specifications of the technical material, as commercially manufactured, and the specifications of the test material used in the toxicity studies;
((3)) the potential long-term risk to herbivorous mammals;
((4)) the fate and behaviour in the environment of the metabolite compounds X and IV;
((5)) the potential risk to fish and aquatic invertebrates for the metabolite compound IV.
The applicant shall submit to the Commission, the Member States and the Authority the information set out in points (1) and (2) by 30 June 2012 and the information set out in points (3), (4) and (5) by 31 December 2013.
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