
Article 1 
Annex I to Directive 91/414/EEC is amended as set out in the Annex to this Directive.
Article 2 
Member States shall bring into force the laws, regulations and administrative provisions necessary to comply with this Directive by 31 July 2011 at the latest. They shall forthwith communicate to the Commission the text of those provisions and a correlation table between those provisions and this Directive.
When Member States adopt those provisions, they shall contain a reference to this Directive or be accompanied by such a reference on the occasion of their official publication. Member States shall determine how such reference is to be made.
Article 3 
This Directive shall enter into force on 1 February 2011.
Article 4 
This Directive is addressed to the Member States.
Done at Brussels, 20 January 2011.
For the Commission
The President
José Manuel BARROSO
ANNEX

The following entry shall be added at the end of the table in Annex I to Directive 91/414/EEC:

No Common Name, Identification Numbers IUPAC Name Purity Entry into force Expiration of inclusion Specific provisions
‘325 BuprofezinCAS No: 953030-84-7CIPAC No: 681 (Z)-2-tert-butylimino-3-isopropyl-5-phenyl-1,3,5-thiadiazinan-4-one ≥ 985 g/kg 1 February 2011 31 January 2021 
PART A Only uses as insecticide and acaricide may be authorised.

PART B For the implementation of the uniform principles of Annex VI the conclusions of the review report on buprofezin, and in particular Appendices I and II thereof, as finalised in the Standing Committee on the Food Chain and Animal Health on 23 November 2010, shall be taken into account.
In this overall assessment Member States shall pay particular attention to:

((a)) the operators’ and workers’ safety and ensure that conditions of use impose adequate personal protective equipment where appropriate;
((b)) the dietary exposure of consumers to the buprofezin (aniline) metabolites in processed food;
((c)) the application of an appropriate waiting period for rotational crops in greenhouses;
((d)) the risk to aquatic organisms and ensure that conditions of use impose adequate risk mitigation measures, where appropriate.
The Member States concerned shall request the submission of confirmatory information as regards the processing and conversion factors for consumer risk assessment.
The Member States concerned shall ensure that the applicant submits such confirmatory information to the Commission by 31 January 2013.’


