Retained EU Law 2015 United Kingdom

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)

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

Conditions for granting licences

  • Obtain a licence by appointing a responsible officer and submitting a detailed application for trading in scheduled substances (Category 1)
s.art005

Conditions for granting registrations

  • Appoint a responsible officer for trade in scheduled substances
s.art006

Cases where a registration is not required

  • Register immediately if your exports of Category 3 drug precursors exceed annual thresholds
s.art008

Criteria for determining the licit purposes of a transaction

  • Provide proof that drug precursor shipments have left the country of export
s.art009

Information required to monitor trade

  • Report scheduled substance use, supply, exports, imports, and intermediary activities
Browse 10 other sections — procedural / definitional / commencement
s.art001

Subject matter

s.art002

Definitions

s.art004

Cases where a licence is not required

s.art007

Conditions for exemptions from certain requirements

s.art010

Conditions for determining the lists of the countries of destination for exports of scheduled substances of Categories 2 and 3

s.art011

Criteria for determining simplified procedures for pre-export notifications

s.art012

Criteria for determining simplified procedures for export authorisations

s.art013

Conditions and requirements concerning the information to be provided on the implementation of the monitoring measures

s.art014

Repeal

s.art015

This Regulation shall enter into force on the third day...

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