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Commission Regulation (EU) No 1141/2010Show full title

Commission Regulation (EU) No 1141/2010 of 7 December 2010 laying down the procedure for the renewal of the inclusion of a second group of active substances in Annex I to Council Directive 91/414/EEC and establishing the list of those substances (Text with EEA relevance)

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Commission Regulation (EU) No 1141/2010 is up to date with all changes known to be in force on or before 12 November 2024. There are changes that may be brought into force at a future date. Help about Changes to Legislation

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Changes and effects yet to be applied to :

  1. Introductory Text

  2. Article 1.Scope

  3. Article 2.Definitions

  4. Article 2a.Determination of existing renewal application

  5. Article 3.Coordinating authority of the Member State

  6. Article 4.Submission of application

  7. Article 5.Format and content of application

  8. Article 6.Checking of application

  9. Article 7.Pre-submission contacts

  10. Article 8.Access to the application

  11. Article 9.Submission of supplementary dossiers

  12. Article 10.Contents of supplementary dossiers

  13. Article 11.Checking of supplementary dossiers

  14. Article 12.Withdrawal and replacement of the applicant

  15. Article 13.Submission of information by third parties

  16. Article 14.Assessment by the rapporteur Member State and the co-rapporteur Member State

  17. Article 15.Comments upon the renewal assessment report and access to that report and to the supplementary summary dossiers

  18. Article 16.Evaluation of the renewal assessment report

  19. Article 17.Review report and presentation of draft acts

  20. Article 18.Access to review report

  21. Article 19.Fees and charges

  22. Article 20.Other charges, levies or fees

  23. Article 21.Entry into force

  24. Signature

    1. ANNEX I

    2. ANNEX II

      Format for application, as provided for in Article 5(1)

      1. The application shall be in writing, signed by the applicant,...

      2. A copy of the application without the updating statement shall...

      3. The application shall be submitted in accordance with the following...

      4. MODEL

        1. 1. Information concerning the applicant

          1. 1.1. Name and address of the applicant including the name of...

        2. 2. Information to facilitate identification

          1. 2.1. Common name (proposed or ISO-accepted) specifying, where relevant, any variants...

          2. 2.2. Chemical name (IUPAC and CAS nomenclature).

          3. 2.3. CAS, CIPAC and EEC numbers (if available).

          4. 2.4. Empirical and structural formula, molecular mass.

          5. 2.5. Specification of purity of the active substance in g/kg which...

          6. 2.6. Classification and labelling of the active substance in accordance with...

      5. An updating statement, as provided for in Article 5(2), shall...

      6. The applicant confirms that the above information submitted on …...

      7. Signature (of the person competent to act for the applicant...

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