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New version applies from 20/04/2009 — introduced by Regulation (EC) No 219/2009. 30 provisions change. Later versions: 30/12/2013, 21/09/2016, 07/07/2018, 13/01/2021, 03/10/2022, 20/02/2023, 03/06/2024, 14/08/2025, 18/09/2026. Article 2 changes in this version: compare with the current text.

Article 2 - Definitions

Article 2
Definitions

For the purposes of this Regulation the following definitions shall apply:

((a))

"scheduled substance" means any substance listed in Annex I, including mixtures and natural products containing such substances. This excludes medicinal products as defined by Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use(13), pharmaceutical preparations, mixtures, natural products and other preparations containing scheduled substances that are compounded in such a way that they cannot be easily used or extracted by readily applicable or economically viable means

((b))

"non-scheduled substance" means any substance which, although not listed in Annex I, is identified as having been used for the illicit manufacture of narcotic drugs or psychotropic substances

((c))

"placing on the market" means any supply, whether in return for payment or free of charge, of scheduled substances in the Community; or the storage, manufacture, production, processing, trade, distribution or brokering of these substances for the purpose of supply in the Community

((d))

"operator" means any natural or legal person engaged in the placing on the market of scheduled substances

((e))

"International Narcotics Control Board" means the Board established by the Single Convention on Narcotic Drugs, 1961, as amended by the 1972 Protocol

((f))

"special licence" means a licence that is granted to a particular type of operator

((g))

"special registration" means a registration that is made for a particular type of operator

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