Commission Directive 2003/79/EC of 13 August 2003 amending Council Directive 91/414/EEC to include Coniothyrium minitans as active substance (Text with EEA relevance)
Modified by
  • Commission Directive 2004/63/ECof 26 April 2004amending Commission Directive 2003/79/EC as regards time limits(Text with EEA relevance), 32004L0063, April 28, 2004
  • Regulation (EC) No 1107/2009 of the European Parliament and of the Councilof 21 October 2009concerning the placing of plant protection products on the market and repealing Council Directives 79/117/EEC and 91/414/EEC, 32009R1107, November 24, 2009
Commission Directive 2003/79/ECof 13 August 2003amending Council Directive 91/414/EEC to include Coniothyrium minitans as active substance(Text with EEA relevance)
Article 1Annex I to Directive 91/414/EEC is amended as set out in the Annex to this Directive.
Article 2Member States shall adopt and publish by 30 June 2004 at the latest the laws, regulations and administrative provisions necessary to comply with this Directive. They shall forthwith inform the Commission thereof.They shall apply those provisions from 1 July 2004.When Member States adopt those provisions, they shall contain a reference to this Directive or shall 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 31.Member States shall review the authorisation for each plant protection product containing Coniothyrium minitans to ensure that the conditions relating to this active substance set out in Annex I to Directive 91/414/EEC are complied with. Where necessary, they shall amend or withdraw authorisations in accordance with Directive 91/414/EEC by 30 June 2004 at the latest.2.For each authorised plant protection product containing Coniothyrium minitans 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 December 2003 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. 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 Coniothyrium minitans as the only active substance, where necessary, amend or withdraw the authorisation by 30 June 2005 at the latest; or(b)in the case of a product containing Coniothyrium minitans as one of several active substances, where necessary, amend or withdraw the authorisation by 30 June 2005 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 4This Directive shall enter into force on 1 January 2004.
Article 5This Directive is addressed to the Member States.
nullANNEXIn Annex I the following row is added at the end of the table.
Further details on identity and specification of active substances are provided in the review report.
NoCommon name, identification NosIUPAC namePurityEntry into forceExpiration of inclusionSpecific provisions
71Coniothyrium minitansStrain CON/M/91-08 (DSM 9660)CIPAC No 614Not applicableFor details on purity and production control see Review Report1 January 200431 December 2013Only uses as fungicide may be authorised.When granting authorisations, the conclusions of the review report on Coniothyrium minitans, and in particular Appendices I and II thereof, as finalised in the Standing Committee on the Food Chain and Animal Health on 4 July 2003 shall be taken into account.In this overall assessment:Member States must pay particular attention to the operator and worker safety and must ensure that the conditions of authorisation include appropriate protective measures.
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Further details on identity and specification of active substances are provided in the review report.
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