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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)

EU Regulation No 2229/2004 · Adopted 3 December 2004 · Extends to United Kingdom

Original text. legislation.gov.uk does not revise this item, so later amendments are not shown here. Changes made to it are listed under each provision when known.

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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Annotations to the whole text

Textual amendments

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Regulation revoked (31.12.2020) by The Plant Protection Products (Miscellaneous Amendments) (EU Exit) Regulations 2019 (S.I. 2019/556), reg. 1(1), Sch. 2 Pt. 1 (with reg. 29(2)) (as amended by S.I. 2020/1376, regs. 1(4), 3(20)); 2020 c. 1, Sch. 5 para. 1(1)

Contents

  1. Chapter I: SUBJECT MATTER AND SCOPE, DEFINITIONS AND THE DESIGNATED MEMBER STATE AUTHORITY Repealed
  2. 1Subject matter and scope Repealed
  3. 2Definitions Repealed
  4. 3Designated Member State authority Repealed
  5. Chapter II: NOTIFICATIONS BY PRODUCERS IN NEW MEMBER STATES OF ACTIVE SUBSTANCES Repealed
  6. 4Notifications by producers in new Member States Repealed
  7. Chapter III: CONDITIONS FOR THE SUBMISSION OF DOSSIERS OF ACTIVE SUBSTANCES AND SUBMISSION OF INFORMATION BY THIRD PARTIES Repealed
  8. 5Submission of dossiers by more than one notifier Repealed
  9. 6Submission of dossiers to the rapporteur Member State Repealed
  10. 7Dossiers for active substances submitted under Directive 98/8/EC Repealed
  11. 8Dossiers for active substances submitted under Regulation (EC) No 1490/2002 Repealed
  12. 9Specific conditions for submissions of dossiers for active substances listed in Part A of Annex I Repealed
  13. 10Specific conditions for submissions of dossiers for active substances listed in Parts B to G of Annex I Repealed
  14. 11Submission of information by third parties Repealed
  15. 12Time limits for submission of dossiers Repealed
  16. 13Non-submission of dossiers Repealed
  17. 14Replacement or withdrawal of notifier Repealed
  18. Chapter IV: EVALUATIONS OF DOSSIERS Repealed
  19. 15General Conditions for evaluations of dossiers Repealed
  20. 16Cooperation between Member States Repealed
  21. 17Specific condition for evaluations of active substances listed in Part A of Annex I Repealed
  22. 18Completeness check of dossiers for substances listed in Parts B to G of Annex I Repealed
  23. 19Specific conditions for evaluations of dossiers for substances listed in Parts B to G of Annex I Repealed
  24. 20General conditions for draft Assessment Reports Repealed
  25. 21Specific conditions for draft Assessment Reports and Recommendations to the Commission for active substances listed in Part A of Annex I Repealed
  26. 22Specific conditions for draft Assessment Reports and Recommendations to the Commission for active substances listed in Parts B to G of Annex I Repealed
  27. 23Replacement of rapporteur Member State Repealed
  28. 24Receipt of and access to the draft assessment report Repealed
  29. 24aEvaluation of the draft assessment report Repealed
  30. 24bActive substances with clear indications that they do not have any harmful effects Repealed
  31. 24cConsultation of the EFSA Repealed
  32. 24dSubmission of additional information after the draft assessment report has been submitted to the EFSA Repealed
  33. 24eWithdrawal by notifier Repealed
  34. 24fActive substance for which there are clear indications of harmful effects Repealed
  35. Chapter V: PRESENTATION OF A DRAFT DIRECTIVE OR DRAFT DECISION CONCERNING ACTIVE SUBSTANCES AND FINALISED REVIEW REPORT Repealed
  36. 25Presentation of a draft directive or draft decision Repealed
  37. 25aView by the EFSA Repealed
  38. 26Finalised review report Repealed
  39. Chapter VI: SUSPENSION OF TIME LIMITS, MEASURES TO BE TAKEN BY MEMBER STATES AND INTERIM PROGRESS REPORTS Repealed
  40. 27Suspension of time limits Repealed
  41. 28Measures taken by Member States Repealed
  42. 29Interim progress report Repealed
  43. Chapter VII: FEES AND OTHER CHARGES Repealed
  44. 30Fees Repealed
  45. 31Other charges, taxes, levies or fees Repealed
  46. Chapter VIII: TEMPORARY AND FINAL PROVISIONS Repealed
  47. 32Temporary measures Repealed
  48. 33Entry into force Repealed
  49. Signature
  50. Annex I: List of active substances (column A), rapporteur Member States (column B) and notifying producers (code identification) (column C) Repealed
  51. PART ADivision PART A Repealed
  52. GROUP 1 Repealed
  53. GROUP 2 Repealed
  54. Group 2.1. Repealed
  55. Group 2.2. Repealed
  56. GROUP 3 Repealed
  57. GROUP 4 Repealed
  58. GROUP 5 Repealed
  59. GROUP 6 Repealed
  60. Group 6.1. Repealed
  61. Group 6.2. Repealed
  62. PART BDivision PART B Repealed
  63. PART CDivision PART C Repealed
  64. PART DDivision PART D Repealed
  65. PART EDivision PART E Repealed
  66. PART FDivision PART F Repealed
  67. PART GDivision PART G Repealed
  68. Annex IIAnnex II Repealed
  69. Annex IIICo-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) Repealed
  70. Annex IVOrganisations 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 Repealed
  71. Annex VDetails to be notified by producers in new Member States Repealed
  72. Annex VICriteria for clear indications of no harmful effects Repealed
  73. 1Division 1 Repealed
  74. 2Division 2 Repealed
  75. Annex VIICriteria for clear indications of harmful effects Repealed
  76. 1Division 1 Repealed
  77. 2Division 2 Repealed

1Subject matter and scopeF1

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2DefinitionsF1

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3Designated Member State authorityF1

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4Notifications by producers in new Member StatesF1

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5Submission of dossiers by more than one notifierF1

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6Submission of dossiers to the rapporteur Member StateF1

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7Dossiers for active substances submitted under Directive 98/8/ECF1

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8Dossiers for active substances submitted under Regulation (EC) No 1490/2002F1

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9Specific conditions for submissions of dossiers for active substances listed in Part A of Annex IF1

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10Specific conditions for submissions of dossiers for active substances listed in Parts B to G of Annex IF1

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11Submission of information by third partiesF1

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12Time limits for submission of dossiersF1

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13Non-submission of dossiersF1

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14Replacement or withdrawal of notifierF1

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15General Conditions for evaluations of dossiersF1

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16Cooperation between Member StatesF1

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17Specific condition for evaluations of active substances listed in Part A of Annex IF1

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18Completeness check of dossiers for substances listed in Parts B to G of Annex IF1

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19Specific conditions for evaluations of dossiers for substances listed in Parts B to G of Annex IF1

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20General conditions for draft Assessment ReportsF1

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21Specific conditions for draft Assessment Reports and Recommendations to the Commission for active substances listed in Part A of Annex IF1

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22Specific conditions for draft Assessment Reports and Recommendations to the Commission for active substances listed in Parts B to G of Annex IF1

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23Replacement of rapporteur Member StateF1

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24Receipt of and access to the draft assessment reportF1

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24aEvaluation of the draft assessment reportF1

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24bActive substances with clear indications that they do not have any harmful effectsF1

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24cConsultation of the EFSAF1

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24dSubmission of additional information after the draft assessment report has been submitted to the EFSAF1

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24eWithdrawal by notifierF1

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24fActive substance for which there are clear indications of harmful effectsF1

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25Presentation of a draft directive or draft decisionF1

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25aView by the EFSAF1

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26Finalised review reportF1

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27Suspension of time limitsF1

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28Measures taken by Member StatesF1

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29Interim progress reportF1

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30FeesF1

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31Other charges, taxes, levies or feesF1

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32Temporary measuresF1

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33Entry into forceF1

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Signature

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PART AF1

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GROUP 1F1

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GROUP 2F1

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Group 2.1.F1

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Group 2.2.F1

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GROUP 3F1

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GROUP 4F1

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GROUP 5F1

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GROUP 6F1

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Group 6.1.F1

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Group 6.2.F1

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PART BF1

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PART CF1

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PART DF1

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PART EF1

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PART FF1

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PART GF1

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Annex IIF1

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Annex IIICo-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)F1

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Annex IVOrganisations 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 paidF1

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Annex VDetails to be notified by producers in new Member StatesF1

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Annex VICriteria for clear indications of no harmful effectsF1

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1F1

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2F1

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Annex VIICriteria for clear indications of harmful effectsF1

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1F1

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2F1

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