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Council Regulation (EC) No 111/2005Show full title

Council Regulation (EC) No 111/2005 of 22 December 2004 laying down rules for the monitoring of trade between the Union and third countries in drug precursors

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  1. Introductory Text

  2. CHAPTER I SUBJECT MATTER AND DEFINITIONS

    1. Article 1.This Regulation lays down rules for the monitoring of trade...

    2. Article 2.For the purposes of this Regulation the following definitions shall...

  3. CHAPTER II MONITORING OF TRADE

    1. SECTION 1 Documentation and labelling

      1. Article 3.All imports, exports or intermediary activities involving scheduled substances, with...

      2. Article 4.The documentation referred to in Article 3 shall be kept...

      3. Article 5.Operators shall ensure that labels are affixed on any packaging...

    2. SECTION 2 Licensing and registration of operators

      1. Article 6.(1) Unless otherwise provided, operators established in the United Kingdom...

      2. Article 7.(1) Unless otherwise provided, operators established in the United Kingdom...

      3. Article 8.(1) When the scheduled substances are entered into the United...

    3. SECTION 3 Provision of information

      1. Article 9.(1) Operators established in the United Kingdom shall notify the...

      2. Article 10.(1) In order to facilitate cooperation between the competent authorities,...

    4. SECTION 4 Pre-export notification

      1. Article 11.(1) All exports of scheduled substances listed in Categories 1...

    5. SECTION 5 Export authorisation

      1. Article 12.(1) Exports of scheduled substances that require a customs declaration,...

      2. Article 13.(1) The application for export authorisations referred to in Article...

      3. Article 14.(1) If the details of the itinerary and means of...

      4. Article 15.Without prejudice to measures adopted in accordance with Article 26(3),...

      5. Article 16.The competent authorities may suspend or revoke an export authorisation...

      6. Article 17.Whenever, under an agreement between the United Kingdom and a...

      7. Article 18.The period of validity of the export authorisation within which...

      8. Article 19.Simplified procedures to grant an export authorisation may be applied...

    6. SECTION 6 Import authorisation

      1. Article 20.Imports of scheduled substances listed in Category 1 of the...

      2. Article 21.(1) The application for the import authorisations referred to in...

      3. Article 22.The import authorisation shall accompany the consignment from the point...

      4. Article 23.Without prejudice to measures adopted in accordance with Article 26(3),...

      5. Article 24.The competent authorities may suspend or revoke the import authorisation...

      6. Article 25.The period of validity of the import authorisation within which...

  4. CHAPTER III POWERS OF COMPETENT AUTHORITIES

    1. Article 26.(1) Without prejudice to Articles 11 to 25 and to...

  5. CHAPTER IV

    1. Article 27.For the purposes of applying this Regulation and without prejudice...

  6. CHAPTER V DELEGATED AND IMPLEMENTING ACTS

    1. Article 28.In addition to the measures referred to in Article 26,...

    2. Article 29.. . . . . . . . . ....

    3. Article 30.(1) The Commission shall be assisted by the Drug Precursors...

    4. Article 30a.The Secretary of State may by regulations make provision to...

    5. Article 30b.A power of the Secretary of State to make regulations...

  7. CHAPTER VI FINAL PROVISIONS

    1. Article 31.Member States shall lay down the rules on penalties applicable...

    2. Article 32.The Secretary of State must draw up a report annually...

    3. Article 32a.The competent authorities of the Member States and the Commission...

    4. Article 33.(1) The processing of personal data by the competent authorities...

    5. Article 34.Regulation (EEC) No 3677/90 is repealed with effect from 18...

    6. Article 35.This Regulation shall enter into force on the 20th day...

  8. Signature

    1. ANNEX

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