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Commission Regulation (EC) No 1451/2007 of 4 December 2007 on the second phase of the 10-year work programme referred to in Article 16(2) of Directive 98/8/EC of the European Parliament and of the Council concerning the placing of biocidal products on the market (Text with EEA relevance) (repealed)

EU Regulation No 1451/2007 · Adopted 4 December 2007 · 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 1451/2007

of 4 December 2007

on the second phase of the 10-year work programme referred to in Article 16(2) of Directive 98/8/EC of the European Parliament and of the Council concerning the placing of biocidal products on the market

(Text with EEA relevance) (repealed)

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Annotations to the whole text

Textual amendments

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Repealed by Commission Delegated Regulation (EU) No 1062/2014 of 4 August 2014 on the work programme for the systematic examination of all existing active substances contained in biocidal products referred to in Regulation (EU) No 528/2012 of the European Parliament and of the Council (Text with EEA relevance).

Contents

  1. 1Subject matter Repealed
  2. 2Definitions Repealed
  3. 3Existing active substances Repealed
  4. 3aProcedure for the declaration of intention to notify Repealed
  5. 3bNotification procedure Repealed
  6. 3cInclusion in, or exclusion from, the review programme Repealed
  7. 4Non-inclusion Repealed
  8. 5Derogation for essential use Repealed
  9. 6Food and Feed Repealed
  10. 7Examination of existing active substances under the review programme Repealed
  11. 8Preparation of the complete dossier Repealed
  12. 9Submission of the complete dossier Repealed
  13. 10Joining and replacing of participants Repealed
  14. 11Withdrawal of participants Repealed
  15. 12Taking over the role of participant Repealed
  16. 13Completeness check of dossiers Repealed
  17. 14Evaluation of dossiers by the Rapporteur Member State Repealed
  18. 15Commission procedures Repealed
  19. 16Access to information Repealed
  20. 17Suspension of procedures Repealed
  21. 18Repeal Repealed
  22. 19Entry into force Repealed
  23. Signature
  24. Annex IAnnex I Repealed
  25. Annex IIAnnex II Repealed
  26. Annex III: Requirements for the complete dossier and the summary dossier Repealed
  27. (a)Division (a) Repealed
  28. (b)The summary dossier must include the following: Repealed
  29. (c)Division (c) Repealed
  30. (d)Division (d) Repealed

1Subject matterF1

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2DefinitionsF1

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3Existing active substancesF1

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3aProcedure for the declaration of intention to notifyF1

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3bNotification procedureF1

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3cInclusion in, or exclusion from, the review programmeF1

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4Non-inclusionF1

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5Derogation for essential useF1

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6Food and FeedF1

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7Examination of existing active substances under the review programmeF1

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8Preparation of the complete dossierF1

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9Submission of the complete dossierF1

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10Joining and replacing of participantsF1

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11Withdrawal of participantsF1

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12Taking over the role of participantF1

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13Completeness check of dossiersF1

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14Evaluation of dossiers by the Rapporteur Member StateF1

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15Commission proceduresF1

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16Access to informationF1

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17Suspension of proceduresF1

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18RepealF1

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19Entry into forceF1

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Signature

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Annex IF1

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Annex IIF1

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(a)F1

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(b)The summary dossier must include the following:F1

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(c)F1

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(d)F1

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