What changes on 30/12/2013
The text in force from 20/04/2009 compared with the text from 30/12/2013.
4 inserted
34 amended
0 deleted
0 moved
Read the act as of 30/12/2013 · other versions: 21/09/2016 · 07/07/2018 · 13/01/2021 · 03/10/2022 · 20/02/2023 · 03/06/2024 · 14/08/2025 · 18/09/2026
Outside any heading
- inserted Article 13a - European database on drug precursors
- inserted Article 13b - Data protection
- inserted Article 14a - Committee procedure
- inserted Article 15a - Exercise of the delegation
- amended Recital 1
- amended Recital 2
- amended Recital 3
- amended Recital 4
- amended Recital 5
- amended Recital 6
- amended Recital 7
- amended Recital 8
- amended Recital 9
- amended Recital 10
- amended Recital 11
- amended Recital 12
- amended Recital 13
- amended Recital 14
- amended Recital 15
- amended Recital 16
- amended Recital 17
- amended Recital 18
- amended Article 1 - Scope and objectives
- amended Article 2 - Definitions
- amended Article 3 - Requirements for the placing on the market of scheduled substances
- amended Article 4 - Customer declaration
- amended Article 5 - Documentation
- amended Article 7 - Labelling
- amended Article 8 - Notification of the competent authorities
- amended Article 9 - Guidelines
- amended Article 10 - Powers and obligations of competent authorities
- amended Article 11 - Cooperation between the Member States and the Commission
- amended Article 13 - Communications from Member States
- amended Article 14 - Implementing acts
- amended Article 15 - Adaptation of Annexes
- amended Article 16 - Information about measures adopted by Member States
- amended Annex I - List of scheduled substances
- amended Annex III - 1.Model declaration relating to individual transactions (category 1 or 2)