Information required to monitor trade
- Submit annual drug precursor reports by 15 February
Retained EU Law
2015
United Kingdom
Commission Implementing Regulation (EU) 2015/1013 of 25 June 2015 laying down rules in respect of Regulation (EC) No 273/2004 of the European Parliament and of the Council on drug precursors and of Council Regulation (EC) No 111/2005 laying down rules for the monitoring of trade between the Union and third countries in drug precursors (Text with EEA relevance)
At a glance
What's here
2 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.
Export and import authorisations
- Return Copy No 2 of simplified export authorisation within 10 working days of expiry
Browse 13 other sections — procedural / definitional / commencement
uri:annex/ii/annotations/1
uri:annex/iii/annotations/2/annotation/2
Subject matter
Definitions
Licence granting procedure
Scope of the licence
Format of the licence
Subsequent changes
Validity, suspension and revocation of licences
Special licences
Registration procedure
Listing of operators and users in the European database on drug precursors
Entry into force and application
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