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roadmaps to reforming the un drug conventions - Beckley Foundation

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If <strong>the</strong> new Article 3 bis were <strong>to</strong> apply <strong>to</strong> Article 30(2)(b)(i), its effect would be that noncommercialsupply or dispensation of small quantities of <strong>drug</strong>s <strong>to</strong> individuals would beexempt from <strong>the</strong> medical prescription requirement, whe<strong>the</strong>r for medical or non-medicaluse. Thus, <strong>the</strong> application of <strong>the</strong> medical prescription requirement would hinge on <strong>the</strong>quantity of <strong>drug</strong>s being supplied and whe<strong>the</strong>r <strong>the</strong> <strong>drug</strong>s were being sold or supplied forfree. It is submitted that, irrespective of <strong>the</strong>se matters, dispensation of <strong>drug</strong>s by medicalprescription is an important safeguard for medical use of <strong>drug</strong>s, as it helps <strong>to</strong> ensure <strong>the</strong>suitability and safety of <strong>drug</strong>s in respect of a person’s medical condition. It is suggested,<strong>the</strong>refore, that <strong>the</strong> most suitable basis for application of <strong>the</strong> medical prescriptionrequirement is whe<strong>the</strong>r <strong>drug</strong>s are supplied or dispensed for medical use, and that <strong>the</strong>quantity of <strong>drug</strong>s and/or commerciality of <strong>the</strong> supply should not be determinative.To achieve this outcome, Article 30(2)(b) would need <strong>to</strong> be exempted from <strong>the</strong> newArticle 3 bis (as proposed above) so that Article 30(2)(b) would continue <strong>to</strong> apply <strong>to</strong>supply or dispensation of small quantities of <strong>drug</strong>s for o<strong>the</strong>r than commercial purposes.In addition, Article 30(2)(b)(i) should be amended directly <strong>to</strong> make it clear that <strong>the</strong>medical prescription requirement applies only in relation <strong>to</strong> medical use of <strong>drug</strong>s.4.14.3 Option 2 – changes <strong>to</strong> Article 30(2)(b)(i)As <strong>un</strong>der Option 1, <strong>the</strong> medical prescription requirement should apply in relation <strong>to</strong> anysupply of <strong>drug</strong>s for medical use for <strong>the</strong> purposes of Option 2. For <strong>the</strong> same reasons asdiscussed above in relation <strong>to</strong> Option 1, Article 30(2)(b)(i) should be amended directly <strong>to</strong>make it clear that <strong>the</strong> medical prescription requirement would apply only in relation <strong>to</strong>medical use of <strong>drug</strong>s. In addition, Article 30(2)(b) should be exempted from <strong>the</strong> newArticle 3 bis (as proposed above) so that medical prescriptions would continue <strong>to</strong> berequired <strong>un</strong>der Article 30(2)(b) for any supply or dispensation of <strong>drug</strong>s for medicalpurposes, irrespective of <strong>the</strong> quantity of <strong>drug</strong>s or whe<strong>the</strong>r <strong>the</strong> supply or dispensationwere commercial.4.14.4 Options 1 and 2 – amendment of Article 30(2)(b)(i)After ‘dispensation of <strong>drug</strong>s <strong>to</strong> individuals’, insert ‘for medical use’.2. The Parties shall also:…Article 30. Trade and Distributionb) (i) Require medical prescriptions for <strong>the</strong> supply, or dispensation of <strong>drug</strong>s <strong>to</strong>individuals for medical use. This requirement need not apply <strong>to</strong> such <strong>drug</strong>s asindividuals may lawfully obtain, use, dispense or administer in connexion with<strong>the</strong>ir duly authorised <strong>the</strong>rapeutic f<strong>un</strong>ctions;123

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