- Y Diweddaraf sydd Ar Gael (Diwygiedig)
- Gwreiddiol (Fel y’i mabwysiadwyd gan yr UE)
Commission Directive 2011/2/EUDangos y teitl llawn
Commission Directive 2011/2/EU of 7 January 2011 amending Council Directive 91/414/EEC to include myclobutanil as active substance and amending Decision 2008/934/EC (Text with EEA relevance)
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- Cyfarwyddebau yn deillio o’r UE
- 2011 No. 2
- Whole Directive without Annexes
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Changes over time for: Commission Directive 2011/2/EU (without Annexes)
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Article 1U.K.
Annex I to Directive 91/414/EEC is amended as set out in the Annex to this Directive.
Article 2U.K.
The line concerning myclobutanil in the Annex to Decision 2008/934/EC is deleted.
Article 3U.K.
Member States shall adopt and publish by 30 November 2011 at the latest the laws, regulations and administrative provisions necessary to comply with this Directive. They shall forthwith communicate to the Commission the text of those provisions and a correlation table between those provisions and this Directive.
They shall apply those provisions from 1 December 2011.
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 4U.K.
1.Member States shall in accordance with Directive 91/414/EEC, where necessary, amend or withdraw existing authorisations for plant protection products containing myclobutanil as an active substance by 30 November 2011.
By that date they shall in particular verify that the conditions in Annex I to that Directive relating to myclobutanil are met, with the exception of those identified in Part B of the entry concerning that active substance, and that the holder of the authorisation has, or has access to, a dossier satisfying the requirements of Annex II to that Directive in accordance with the conditions of Article 13 of that Directive.
2.By way of derogation from paragraph 1, for each authorised plant protection product containing myclobutanil as either the only active substance or as one of several active substances all of which were listed in Annex I to Directive 91/414/EEC by 31 May 2011 at the latest, Member States shall re-evaluate the product in accordance with the uniform principles provided for in Annex VI to Directive 91/414/EEC, on the basis of a dossier satisfying the requirements of Annex III to that Directive and taking into account Part B of the entry in Annex I to that Directive concerning myclobutanil. On the basis of that evaluation, they shall determine whether the product satisfies the conditions set out in Article 4(1)(b), (c), (d) and (e) of Directive 91/414/EEC.
Following that determination Member States shall:
(a)in the case of a product containing myclobutanil as the only active substance, where necessary, amend or withdraw the authorisation by 31 May 2015 at the latest; or
(b)in the case of a product containing myclobutanil as one of several active substances, where necessary, amend or withdraw the authorisation by 31 May 2015 or by the date fixed for such an amendment or withdrawal in the respective Directive or Directives which added the relevant substance or substances to Annex I to Directive 91/414/EEC, whichever is the latest.
Article 5U.K.
This Directive shall enter into force on 1 June 2011.
Article 6U.K.
This Directive is addressed to the Member States.
Done at Brussels, 7 January 2011.
For the Commission
The President
José Manuel Barroso
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