equirements and supply limits would not have any application <strong>to</strong> supply, use orconsumption of <strong>drug</strong>s for non-medical and non-scientific purposes. Therefore, <strong>the</strong>ywould not facilitate moni<strong>to</strong>ring of, or help <strong>to</strong> prevent over-supply of <strong>drug</strong>s <strong>to</strong>, regulatednon-medical and non-scientific domestic markets, or help <strong>to</strong> prevent diversion fromthose markets <strong>to</strong> illicit markets. It may be difficult <strong>to</strong> justify <strong>the</strong> discrepancy between <strong>the</strong>reporting and control measures required for medical and scientific markets incomparison with regulated non-medical and non-scientific markets, since <strong>the</strong> latter seemjust as likely <strong>to</strong> be a source of diversion <strong>to</strong> illicit markets. In addition, this would beinconsistent with <strong>the</strong> existing approach <strong>un</strong>der <strong>the</strong> Convention, which currently requires<strong>the</strong> furnishing of separate estimates in respect of <strong>the</strong> use of coca leaves for preparation offlavouring agents <strong>un</strong>der Article 27, and which previously required <strong>the</strong> furnishing ofseparate estimates for permitted non-medical or quasi-medical uses of <strong>drug</strong>s pursuant <strong>to</strong>transitional reservations <strong>un</strong>der Article 49, when <strong>the</strong>se reservations were still in force.Therefore, it is submitted that <strong>the</strong> better approach would be for <strong>the</strong> estimate system,statistical report requirements and supply limits <strong>to</strong> be extended <strong>to</strong> non-medical and nonscientificproduction, manufacture, use, s<strong>to</strong>cks and consumption of <strong>drug</strong>s. Under thisapproach, Article 19 would need <strong>to</strong> be amended such that Parties would be required <strong>to</strong>furnish estimates of quantities of <strong>drug</strong>s <strong>to</strong> be consumed, used, held in s<strong>to</strong>cks, producedand manufactured for both medical and scientific purposes and o<strong>the</strong>r purposes, andwould be required <strong>to</strong> limit <strong>the</strong> quantities actually consumed, used, held in s<strong>to</strong>cks,produced and manufactured for medical and scientific purposes and o<strong>the</strong>r purposes <strong>to</strong><strong>the</strong> relevant estimates for those purposes. 128 Similarly, Article 20 would need <strong>to</strong> beamended <strong>to</strong> require Parties <strong>to</strong> furnish statistical returns in relation <strong>to</strong> production,manufacture, use, s<strong>to</strong>cks and consumption of <strong>drug</strong>s for both medical and scientificpurposes and o<strong>the</strong>r purposes. In addition, Article 21 would need <strong>to</strong> be amended <strong>to</strong> addquantities consumed for non-medical and non-scientific purposes, and quantities used<strong>to</strong> manufacture o<strong>the</strong>r <strong>drug</strong>s, Schedule III preparations and <strong>un</strong>controlled substances fornon-medical and non-scientific purposes <strong>to</strong> <strong>the</strong> quantities <strong>to</strong> be taken in<strong>to</strong> acco<strong>un</strong>t <strong>un</strong>derArticle 21(1) in determining manufacture and import limits for each <strong>drug</strong>. (Theproposed amendments <strong>to</strong> Articles 20 and 21 are discussed in more detail in sections 4.8and 4.9 below.)The ‘<strong>to</strong>tals of <strong>the</strong> estimates’ which are calculated <strong>un</strong>der Article 19(2) would need <strong>to</strong> beextended <strong>to</strong> estimates of quantities <strong>to</strong> be consumed, used, held in s<strong>to</strong>cks, and producedand manufactured for non-medical and non-scientific, as well as medical and scientificpurposes. This would be <strong>to</strong> ensure that <strong>the</strong> ‘<strong>to</strong>tal of <strong>the</strong> estimates’ would take in<strong>to</strong>acco<strong>un</strong>t both non-medical/non-scientific and medical/scientific estimates for <strong>the</strong>purposes of <strong>the</strong> provision in Article 21(4) for <strong>the</strong> INCB <strong>to</strong> embargo fur<strong>the</strong>r exports <strong>to</strong> aco<strong>un</strong>try or terri<strong>to</strong>ry if quantities exported <strong>to</strong> it exceed its <strong>to</strong>tal of estimates, and <strong>the</strong>128But note that <strong>the</strong> existing requirements in relation <strong>to</strong> special s<strong>to</strong>cks would not need <strong>to</strong> be changed,as special s<strong>to</strong>cks (i.e. s<strong>to</strong>cks held for special government purposes and exceptional circumstances)would still only be kept for medical and scientific purposes <strong>un</strong>der Option 2.101
prohibition in Article 31(1)(b) against Parties knowingly permitting <strong>the</strong> export of <strong>drug</strong>s<strong>to</strong> a co<strong>un</strong>try or terri<strong>to</strong>ry beyond its <strong>to</strong>tal of estimates.The changes <strong>to</strong> <strong>the</strong> system proposed <strong>un</strong>der this approach would mean that <strong>the</strong> estimateand statistical return requirements would continue <strong>to</strong> enable <strong>the</strong> INCB <strong>to</strong> moni<strong>to</strong>rco<strong>un</strong>tries’ and terri<strong>to</strong>ries’ medical and scientific <strong>drug</strong> requirements, and assist <strong>the</strong> INCB<strong>to</strong> ensure an adequate supply of <strong>drug</strong>s for <strong>the</strong>se purposes. In addition, <strong>the</strong>serequirements, and <strong>the</strong> limits on manufacture and import, would enable <strong>the</strong> INCB <strong>to</strong>moni<strong>to</strong>r <strong>the</strong> supply and consumption of <strong>drug</strong>s for licit non-medical and non-scientificpurposes, as well as medical and scientific purposes, and assist <strong>the</strong> INCB <strong>to</strong> preven<strong>to</strong>ver-supply <strong>to</strong> both markets. This approach would also be consistent with <strong>the</strong> existingrequirement for estimates <strong>to</strong> be furnished in respect of <strong>the</strong> use of coca leaf as aflavouring agent, and <strong>the</strong> previous requirement for estimates <strong>to</strong> be furnished in respec<strong>to</strong>f permitted non-medical and quasi-medical use of <strong>drug</strong>s, as discussed above.To change <strong>the</strong> estimate system in <strong>the</strong> manner proposed, Article 19(1) would need <strong>to</strong> beamended <strong>to</strong> specify that separate estimates must be furnished in respect of <strong>the</strong> quantitiesset out in subparagraphs (a) (b), (c) and (f) and (h) of that article for both medical andscientific purposes, and for o<strong>the</strong>r purposes. This would have <strong>the</strong> effect of ensuring that<strong>the</strong> <strong>to</strong>tals of <strong>the</strong> estimates calculated <strong>un</strong>der Article 19(2) would be based on medical andscientific estimates and non-medical and non-scientific estimates, without <strong>the</strong> need fordirect amendment of that provision, as Article 19(2) currently requires <strong>the</strong> <strong>to</strong>tals ofestimates <strong>to</strong> be based on <strong>the</strong> estimates set out in subparagraphs (a) (b), (c), (d) (f) and (h).Subparagraph (d) requires estimates of quantities of <strong>drug</strong>s needed for special s<strong>to</strong>cks,which are amo<strong>un</strong>ts held by governments for special government purposes (including,particularly, military purposes) and exceptional circumstances (e.g. large-scaleepidemics and earthquakes). 129 It is likely that all purposes for which special s<strong>to</strong>cks maybe used would be medical or scientific.Unlike subparagraph (a) of Article 19(1), subparagraphs (b), (c), (f) and (h) as currentlydrafted, do not specify that estimates are only required in respect of medical or scientificpurposes. However, this is clearly <strong>the</strong> case as, by virtue of Article 4(c), only medical orscientific use of <strong>drug</strong>s is permitted. The removal of Article 4(c) from <strong>the</strong> Convention asproposed <strong>un</strong>der Option 2 would mean that <strong>the</strong> required estimates in <strong>the</strong>sesubparagraphs would extend <strong>to</strong> non-medical and non-scientific purposes, withoutamendment of <strong>the</strong> provision. However, it is proposed that <strong>the</strong> subparagraphs should bedirectly amended <strong>to</strong> make it clear that separate estimates would be required for medicaland scientific purposes, and for o<strong>the</strong>r purposes, ra<strong>the</strong>r than aggregate estimates for allpurposes.In addition, as discussed in more detail above, <strong>the</strong> definition of ‘s<strong>to</strong>cks’ in Article 1(1)(x)would need <strong>to</strong> be amended <strong>to</strong> remove its current limitation <strong>to</strong> amo<strong>un</strong>ts held forconsumption for ‘medical and scientific purposes’, and <strong>the</strong> definition of ‘consumed’ in1291961 Convention, article 1(1)(w); 1961 Commentary, pp. 32–33.102
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ROADMAPS TO REFORMINGTHE UN DRUG CO
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ContentsPreface ...................
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PrefaceTHE IDEA FOR this Report cam
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PART I. POSSIBLE ROADMAPS
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hope for serious progress, but we c
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We do not underestimate the difficu
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also imposes requirements concernin
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domestic market, just as producers
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Protocol strengthened some provisio
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ut considerably less potency than s
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has announced its intention to reac
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objected to. Concerning the 1971 tr
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Table 2. Summary of reservations to
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Reservations about traditional use
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As Swaine notes, ‘the Vienna Conv
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unhappy about a country implementin
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Preemption by a new ‘single conve
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and their effort was rejected by a
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national or subnational level. Proh
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Chapter 5. Proposed treaty amendmen
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Article 1. DefinitionsExcept where
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Article 36 - penal provisionsIn Art
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Article 7. Special Provisions regar
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and to ensure adequate supplies of
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Article 1 − definition of ‘cons
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Article 19 - estimates of drug requ
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Article 21. Limitation of Manufactu
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contrary to a law or regulation ado
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4. The Parties shall furnish to the
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2. In subparagraph (b):a) after ‘
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obligations on Parties in respect o
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penalise preparatory acts in connec
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accordance with subparagraph (a) of
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Article 3(1)(c)(iii) warrants speci
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6.1.2. Option 1 - changes to the 19
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uncertainty. Accordingly, Article 3
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Consequently, Parties would also no
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…4. d) The Parties may provide, e