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Commission Regulation (EC) No 2229/2004Show full title

Commission Regulation (EC) No 2229/2004 of 3 December 2004 laying down further detailed rules for the implementation of the fourth stage of the programme of work referred to in Article 8(2) of Council Directive 91/414/EEC (Text with EEA relevance) (revoked)

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  1. Introductory Text

  2. CHAPTER I SUBJECT MATTER AND SCOPE, DEFINITIONS AND THE DESIGNATED MEMBER STATE AUTHORITY

    1. Article 1.Subject matter and scope

    2. Article 2.Definitions

    3. Article 3.Designated Member State authority

  3. CHAPTER II NOTIFICATIONS BY PRODUCERS IN NEW MEMBER STATES OF ACTIVE SUBSTANCES

    1. Article 4.Notifications by producers in new Member States

  4. CHAPTER III CONDITIONS FOR THE SUBMISSION OF DOSSIERS OF ACTIVE SUBSTANCES AND SUBMISSION OF INFORMATION BY THIRD PARTIES

    1. Article 5.Submission of dossiers by more than one notifier

    2. Article 6.Submission of dossiers to the rapporteur Member State

    3. Article 7.Dossiers for active substances submitted under Directive 98/8/EC

    4. Article 8.Dossiers for active substances submitted under Regulation (EC) No 1490/2002

    5. Article 9.Specific conditions for submissions of dossiers for active substances listed in Part A of Annex I

    6. Article 10.Specific conditions for submissions of dossiers for active substances listed in Parts B to G of Annex I

    7. Article 11.Submission of information by third parties

    8. Article 12.Time limits for submission of dossiers

    9. Article 13.Non-submission of dossiers

    10. Article 14.Replacement or withdrawal of notifier

  5. CHAPTER IV EVALUATIONS OF DOSSIERS

    1. Article 15.General Conditions for evaluations of dossiers

    2. Article 16.Cooperation between Member States

    3. Article 17.Specific condition for evaluations of active substances listed in Part A of Annex I

    4. Article 18.Completeness check of dossiers for substances listed in Parts B to G of Annex I

    5. Article 19.Specific conditions for evaluations of dossiers for substances listed in Parts B to G of Annex I

    6. Article 20.General conditions for draft Assessment Reports

    7. Article 21.Specific conditions for draft Assessment Reports and Recommendations to the Commission for active substances listed in Part A of Annex I

    8. Article 22.Specific conditions for draft Assessment Reports and Recommendations to the Commission for active substances listed in Parts B to G of Annex I

    9. Article 23.Replacement of rapporteur Member State

    10. Article 24. Receipt of and access to the draft assessment report

    11. Article 24a. Evaluation of the draft assessment report

    12. Article 24b. Active substances with clear indications that they do not have any harmful effects

    13. Article 24c. Consultation of the EFSA

    14. Article 24d. Submission of additional information after the draft assessment report has been submitted to the EFSA

    15. Article 24e. Withdrawal by notifier

    16. Article 24f. Active substance for which there are clear indications of harmful effects

  6. CHAPTER V PRESENTATION OF A DRAFT DIRECTIVE OR DRAFT DECISION CONCERNING ACTIVE SUBSTANCES AND FINALISED REVIEW REPORT

    1. Article 25. Presentation of a draft directive or draft decision

    2. Article 25a. View by the EFSA

    3. Article 26.Finalised review report

  7. CHAPTER VI SUSPENSION OF TIME LIMITS, MEASURES TO BE TAKEN BY MEMBER STATES AND INTERIM PROGRESS REPORTS

    1. Article 27.Suspension of time limits

    2. Article 28.Measures taken by Member States

    3. Article 29.Interim progress report

  8. CHAPTER VII FEES AND OTHER CHARGES

    1. Article 30.Fees

    2. Article 31.Other charges, taxes, levies or fees

  9. CHAPTER VIII TEMPORARY AND FINAL PROVISIONS

    1. Article 32.Temporary measures

    2. Article 33.Entry into force

  10. Signature

    1. ANNEX I

      List of active substances (column A), rapporteur Member States (column B) and notifying producers (code identification) (column C)

      1. PART A GROUP 1 LEAD RAPPORTEUR: IRELAND Active substance Rapporteur Member State...

        1. GROUP 1

        2. GROUP 2

          1. Group 2.1.

          2. Group 2.2.

        3. GROUP 3

        4. GROUP 4

        5. GROUP 5

        6. GROUP 6

          1. Group 6.1.

          2. Group 6.2.

      2. PART B LEAD RAPPORTEUR: AUSTRIA RAPPORTEUR: AUSTRIA (The Czech Republic, Poland and...

      3. PART C LEAD RAPPORTEURS: NETHERLANDS, SWEDEN Active substance Rapporteur Member State Notifier...

      4. PART D LEAD RAPPORTEUR: GERMANY Active substance Rapporteur Member State Notifier (A)...

      5. PART E Active substance Rapporteur Member State Notifier (A) (B) (C) Aluminium...

      6. PART F LEAD RAPPORTEUR: NETHERLANDS Active substance Rapporteur Member State Notifier (A)...

      7. PART G LEAD RAPPORTEUR: POLAND Active substance Rapporteur Member State Notifier (A)...

    2. ANNEX II

    3. ANNEX III

      Co-ordinating authority in the Member States (more details are available at the following webside: http://www.europa.eu.int/comm/food/fs/ph_ps/pro/index_en.htm)

      1. AUSTRIA Bundesamt für Ernährungssicherheit Landwirtschaftliche Untersuchungen und Forschung Wien Spargelfeldstraße...

    4. ANNEX IV

      Organisations in the Member States to be contacted concerning further details on the payment of the fees referred to in Article 30 and to which such fees have to be paid

      1. AUSTRIA Bundesamt für Ernährungssicherheit Landwirtschaftliche Untersuchungen und Forschung Wien Spargelfeldstraße...

    5. ANNEX V

      Details to be notified by producers in new Member States

      1. The notification must be made on paper and by e-mail....

      2. The notification shall contain the following information:

      3. IDENTIFICATION DATA ON THE NOTIFIER Manufacturer of the active substance...

    6. ANNEX VI

      Criteria for clear indications of no harmful effects

      1. An active substance shall be considered as fulfilling the requirement,...

      2. 1. The active substance satisfies the following criteria:

      3. 2. At least one supported representative use of the active substance...

    7. ANNEX VII

      Criteria for clear indications of harmful effects

      1. An active substance shall be considered as fulfilling the requirement,...

      2. 1. As regards the active substance, the existing evidence is not...

      3. 2. As regards each supported representative use, at least one of...

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