Retained EU Law 2005 United Kingdom

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

At a glance

What's here

5 compliance obligations

What this Act requires

Sections that create concrete duties on businesses or carry penalties. Procedural and definitional sections are folded into the “Browse other sections” expander at the bottom of each group. Click any section title to read the source text on legislation.gov.uk.

s.art003

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

  • Document all imports, exports and intermediary activities involving drug precursors with specific details
s.art004

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

  • Keep records of drug precursor transactions for 3 years and make them available for inspection
s.art005

Operators shall ensure that labels are affixed on any packaging...

  • Label packaging containing scheduled substances
s.art008

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

  • Demonstrate licit purpose for scheduled substances entering the UK
s.art009

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

  • Notify authorities immediately of suspicious drug precursor transactions
Browse 32 other sections — procedural / definitional / commencement
s.art001

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

s.art002

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

s.art006

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

s.art007

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

s.art010

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

s.art011

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

s.art012

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

s.art013

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

s.art014

(1) If the details of the itinerary and means of...

s.art015

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

s.art016

The competent authorities may suspend or revoke an export authorisation...

s.art017

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

s.art018

The period of validity of the export authorisation within which...

s.art019

Simplified procedures to grant an export authorisation may be applied...

s.art020

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

s.art021

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

s.art022

The import authorisation shall accompany the consignment from the point...

s.art023

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

s.art024

The competent authorities may suspend or revoke the import authorisation...

s.art025

The period of validity of the import authorisation within which...

s.art026

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

s.art027

For the purposes of applying this Regulation and without prejudice...

s.art028

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

s.art030

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

s.art030

The Secretary of State may by regulations make provision to...

s.art030

A power of the Secretary of State to make regulations...

s.art031

Member States shall lay down the rules on penalties applicable...

s.art032

The Secretary of State must draw up a report annually...

s.art032

The competent authorities of the Member States and the Commission...

s.art033

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

s.art034

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

s.art035

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

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