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Commission Regulation (EC) No 1277/2005 of 27 July 2005 laying down implementing rules for Regulation (EC) No 273/2004 of the European Parliament and of the Council on drug precursors and for Council Regulation (EC) No 111/2005 laying down rules for the monitoring of trade between the Community and third countries in drug precursors (Text with EEA relevance) (repealed)

EU Regulation No 1277/2005 · Adopted 27 July 2005 · 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 1277/2005

of 27 July 2005

laying down implementing rules for Regulation (EC) No 273/2004 of the European Parliament and of the Council on drug precursors and for Council Regulation (EC) No 111/2005 laying down rules for the monitoring of trade between the Community and third countries in drug precursors

(Text with EEA relevance) (repealed)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Repealed by Commission Delegated Regulation (EU) 2015/1011 of 24 April 2015 supplementing Regulation (EC) No 273/2004 of the European Parliament and of the Council on drug precursors and Council Regulation (EC) No 111/2005 laying down rules for the monitoring of trade between the Union and third countries in drug precursors, and repealing Commission Regulation (EC) No 1277/2005 (Text with EEA relevance).

Contents

  1. Chapter I: GENERAL PROVISIONS Repealed
  2. 1Article 1 Repealed
  3. 2Article 2 Repealed
  4. Chapter II: RESPONSIBLE OFFICER Repealed
  5. 3Article 3 Repealed
  6. 4Article 4 Repealed
  7. Chapter III: LICENSING AND REGISTRATION OF OPERATORS Repealed
  8. 5Article 5 Repealed
  9. 6Article 6 Repealed
  10. 7Article 7 Repealed
  11. 8Article 8 Repealed
  12. 9Article 9 Repealed
  13. 10Article 10 Repealed
  14. 11Article 11 Repealed
  15. 12Article 12 Repealed
  16. 13Article 13 Repealed
  17. 14Article 14 Repealed
  18. 15Article 15 Repealed
  19. 16Article 16 Repealed
  20. Chapter IV: PROVISION OF INFORMATION Repealed
  21. 17Article 17 Repealed
  22. 18Article 18 Repealed
  23. 19Article 19 Repealed
  24. Chapter V: PRE-EXPORT NOTIFICATION Repealed
  25. 20Article 20 Repealed
  26. 21Article 21 Repealed
  27. Chapter VI: EXPORT/IMPORT AUTHORISATION Repealed
  28. 22Article 22 Repealed
  29. 23Article 23 Repealed
  30. 24Article 24 Repealed
  31. 25Article 25 Repealed
  32. 26Article 26 Repealed
  33. 27Article 27 Repealed
  34. Chapter VII: FINAL PROVISIONS Repealed
  35. 28Article 28 Repealed
  36. 29Article 29 Repealed
  37. 30Article 30 Repealed
  38. 31Article 31 Repealed
  39. 32Article 32 Repealed
  40. Signature
  41. Annex I Repealed
  42. Annex IIAnnex II Repealed
  43. Annex III Repealed
  44. Annex IV Repealed
  45. 1List of countries referred to in Article 20 for which a pre-export notification is required for exports of scheduled substances of category 2 of the Annex to Regulation (EC) No 111/2005 Repealed
  46. 2List of countries referred to in Articles 20 and 22 for which a pre-export notification and an export authorisation is required for exports of scheduled substances of category 3 of the Annex to Regulation (EC) No 111/2005 Repealed
  47. Annex V Repealed
  48. Annex VI Repealed
  49. Repealed
  50. Notes Repealed
  51. Annex VII Repealed

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Signature

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Annex IIF1

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1List of countries referred to in Article 20 for which a pre-export notification is required for exports of scheduled substances of category 2 of the Annex to Regulation (EC) No 111/2005F1

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2List of countries referred to in Articles 20 and 22 for which a pre-export notification and an export authorisation is required for exports of scheduled substances of category 3 of the Annex to Regulation (EC) No 111/2005F1

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