Requirements for the placing on the market of scheduled substances
- Appoint a responsible officer and obtain a licence or registration for drug precursors
Retained EU Law
2004
United Kingdom
Regulation (EC) No 273/2004 of the European Parliament and of the Council of 11 February 2004 on drug precursors (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.
Customer declaration
- Obtain customer declarations for category 1 and 2 scheduled substances
Documentation
- Document all transactions involving scheduled drug precursor substances
Labelling
- Label scheduled drug precursors before supply with official names
Notification of the competent authorities
- Notify authorities of suspicious transactions and provide transaction summaries
Browse 17 other sections — procedural / definitional / commencement
Scope and objectives
Definitions
Exemptions
Guidelines
Powers and obligations of competent authorities
Cooperation between the Member States and the Commission
Penalties
Report to International Narcotics Control Board
European database on drug precursors
Data protection
Implementing acts
Committee procedure
Adaptation of Annexes
Regulations
Information about measures adopted by Member States
Repeals
Entry into force
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