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Introductory Text
Article 1. Scope and objectives
Article 2.Definitions
Article 3.Requirements for the placing on the market of scheduled substances
Article 4.Customer declaration
Article 5.Documentation
Article 6.Exemptions
Article 7.Labelling
Article 8. Notification of the competent authorities
Article 9.Guidelines
Article 10.Powers and obligations of competent authorities
Article 11.Cooperation between the Member States and the Commission
Article 12.Penalties
Article 13. Communications from Member States
Article 13a. European database on drug precursors
Article 13b. Data protection
Article 14. Implementing acts
Article 14a. Committee procedure
Article 15. Adaptation of Annexes
Article 15a. Exercise of the delegation
Article 16. Information about measures adopted by Member States
Article 17.Repeals
Article 18.Entry into force
Signature
ANNEX I
List of scheduled substances
ANNEX II
ANNEX III
1. Model declaration relating to individual transactions (category 1 or 2)...
2. Model declaration relating to multiple transactions (category 2)