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roadmaps to reforming the un drug conventions - Beckley Foundation

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<strong>the</strong> export of <strong>drug</strong>s <strong>to</strong> a co<strong>un</strong>try or terri<strong>to</strong>ry except within <strong>the</strong> limits of <strong>the</strong> <strong>to</strong>tal of <strong>the</strong>estimates for that co<strong>un</strong>try or terri<strong>to</strong>ry. 130Paragraph 1 of Article 20 provides that <strong>the</strong> INCB must supply forms <strong>to</strong> Parties on which<strong>the</strong> statistical returns are <strong>to</strong> be provided. Current statistical return forms require specificinformation about more than 50 different <strong>drug</strong>s. 131 According <strong>to</strong> <strong>the</strong> 1961 Commentary,<strong>the</strong> INCB also has an implied right <strong>to</strong> request statistical returns from non-Parties <strong>to</strong> <strong>the</strong>Convention. 132As with ‘consumed’ in Article 19, ‘consumption’ in subparagraph (1)(c) of Article 20 has<strong>the</strong> specific meaning given in Article 1(2) – supply <strong>to</strong> a person or enterprise for retaildistribution, medical use or scientific research.Similar obligations <strong>to</strong> furnish statistical returns in respect of psychotropic substances areimposed on Parties by Article 16(4) of <strong>the</strong> 1971 Convention.4.8.2 Option 2 – changes <strong>to</strong> Article 20As discussed above and below, it is proposed that Article 19 should be amended <strong>to</strong>require Parties <strong>to</strong> furnish separate estimates for medical/scientific markets, and nonmedical/non-scientificmarkets in <strong>drug</strong>s, and that Article 21 should be amended <strong>to</strong>require non–medical or scientific use, consumption and additions <strong>to</strong> s<strong>to</strong>cks of <strong>drug</strong>s <strong>to</strong>be taken in<strong>to</strong> acco<strong>un</strong>t in determining manufacture and import limits. Therefore, <strong>to</strong>ensure that statistical returns would continue <strong>to</strong> enable assessment of whe<strong>the</strong>r estimateshave been exceeded and determination of manufacture and import limits, and <strong>to</strong>facilitate moni<strong>to</strong>ring of non-medical/non-scientific markets in <strong>drug</strong>s, as well asmedical/scientific markets, it is also proposed that Article 20(1) should be amended <strong>to</strong>require Parties <strong>to</strong> furnish separate statistical returns in respect of production,manufacture, use and consumption of <strong>drug</strong>s for medical or scientific purposes, as wellas for non-medical and non-scientific purposes.Article 20(1) does not specify that statistical returns are only required in respect ofproduction, manufacture, use and consumption of <strong>drug</strong>s for medical or scientificpurposes; however, this is <strong>the</strong> case by virtue of Article 4(c), because only medical orscientific production, manufacture, use and consumption of <strong>drug</strong>s is permitted. Theremoval of Article 4(c) from <strong>the</strong> Convention would mean that <strong>the</strong> requirements inArticle 20(1) for provision of statistical returns would extend <strong>to</strong> non-medical and nonscientificproduction, manufacture, use and consumption of <strong>drug</strong>s, without amendmen<strong>to</strong>f <strong>the</strong> provision. However, Article 20(1) should be directly amended <strong>to</strong> make it clear that1301961 Commentary, p. 243.131International Narcotics Control Board. Form C, Annual statistics on production, manufacture,consumption, s<strong>to</strong>cks and seizures of narcotic <strong>drug</strong>s.http://www.incb.org/pdf/forms/form_c/Form_C_14edition_09/Form_C_14_1209_English.pdf(accessed 8 July, 2012).1321961 Commentary, p. 244.105

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