Commission Delegated Regulation (EU) No 2015/1011 of 24 April 2015

Notifying member
United Kingdom
Title
Commission Delegated Regulation (EU) No 2015/1011 of 24 April 2015
First published
26/06/2018
First EIF
31/12/2020
Latest published
In force to
Latest notification
G/LIC/N/3/GBR/3
Product categories
List of products subject to licensing
Attachment
Nature of licensing

Non-automatic

Administrative purpose/measure being implemented
  • Pursue obligations under the UN Charter and other international treaties (i.e. CITES, Basel Convention, Rotterdam Convention, UNSC Resolutions etc.)
  • Protect human, animal or plant life and health; protect environment
Administrative body(ies) for submission of applications
Drugs and Firearms Licensing Unit
2 Marsham St, LONDON, SW1P 4DF, UK
https://www.gov.uk/guidance/precursor-chemical-licensing
020 7035 6330

dflu.ie@homeoffice.gov.uk

Contact point for information on eligibility

Same as the "Administrative bodies"

Expected duration of licensing procedure
Ongoing
Found by secretariat
No
Related document symbols
  • G/LIC/N/2/GBR/8
  • G/LIC/N/2/GBR/8/Corr.1
Source
Notes
  • Previously notified in N1GBR1

    Retained EU Law -

    Some European Union law was retained in UK law by virtue of the European Union (Withdrawal) Act 2018 and the European Union (Withdrawal Agreement) Act 2020, with minor modifications to ensure operability.

    Specific arrangements may apply in Northern Ireland including by virtue of the Protocol on Ireland/Northern Ireland. The full text of the Protocol on Ireland/Northern Ireland can be accessed via: https://www.gov.uk/government/publications/new-withdrawal-agreement-and-political-declaration. Further details on the operation of the Protocol on Ireland/Northern Ireland can be found at: https://www.gov.uk/government/publications/the-northern-ireland-protocol.


    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.


  • G/LIC/N/2/GBR/8


    The Drug Precursors Licensing regime is an established regime which derives from the requirements of wider international obligations under the United Nations Convention against Illicit Traffic in Narcotic Drugs and Psychotropic Substances 1988.

    This will mean that companies trading in drug precursors will be required to apply to the Home Office Drugs and Firearms Licensing Unit for:

    • Domestic Licences and Registrations – when possessing certain categories of drug precursor chemicals.

    • Import and Export Licences – when trading in certain categories of chemicals.

    • Pre-export notification – when trading in certain categories of chemicals.

    The full licensing requirements and processes can be found at the following link:

    https://www.gov.uk/guidance/precursor-chemical-licensing


    Products:- Full list in the annex and can be found in the following link: https://www.gov.uk/government/publications/precursor-chemical-import-and-export-authorisation-wallchart


  • G/LIC/N/2/GBR/8/Corr.1


    Administrative purpose/measure being implemented: Protect human, animal or plant life and health; protect environment; and Pursue obligations under the UN Charter and other international treaties (i.e., CITES, Basel Convention, Rotterdam Convention, UNSC Resolutions etc.)