The challenge of responding to a more globally joined-up, dynamic, and innovative drug market: Reflections from the EMCDDA´s 2018 analysis of the European drug situation

P. Griffiths, Eoghan Quigley, L. Vandam, Jane Mounteney
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引用次数: 2

Abstract

Dusunen Adam The Journal of Psychiatry and Neurological Sciences, Volume 31, Number 3, September 2018 Each year in the European Drug Report (EDR), the European Monitoring Centre for Drugs and Drug Addiction (EMCDDA) produces an overview of trends and developments in the drug situation. Founded in 1993, and based in Lisbon, Portugal, since 1995, the EMCDDA is the designated reference point for drugrelated information in the European Union (EU). It works with all EU member states as well as, by special agreement, with Norway and Turkey. Data are collected annually for a set of standardised indicators that cover both drug demand and drug supply measures. In addition, the EMCDDA, together with Europol, is responsible for the EU’s early warning system on new psychoactive substances (NPS). This three-step mechanism allows for the sharing of information on non-controlled psychoactive substances appearing in Europe that may pose a risk to health similar to drugs controlled under the United Nations Conventions. Should it be merited, information provided to the early warning system may trigger a risk assessment, which is conducted by the EMCDDA’s Scientific Committee. This exercise can potentially lead to a decision for fast track control measures being introduced across the EU. In this editorial, we consider how a more globally joined-up, dynamic and innovative drug market has impacted on drug availability and on drug use problems. In doing so, we build on the commentary and analysis of the Dusunen Adam The Journal of Psychiatry and Neurological Sciences 2018;31:231-237 Guest Editorial / Misafir Editoryal DOI: 10.5350/DAJPN20183103001
应对更全球化、更有活力和更创新的药品市场的挑战:EMCDDA 2018年欧洲药品形势分析的思考
《精神病学和神经科学杂志》,第31卷,第3期,2018年9月每年欧洲药物报告(EDR)中,欧洲药物和药物成瘾监测中心(EMCDDA)都会对药物形势的趋势和发展进行概述。EMCDDA成立于1993年,总部设在葡萄牙里斯本,自1995年以来一直是欧盟(EU)药品相关信息的指定参考点。它与所有欧盟成员国合作,并通过特殊协议与挪威和土耳其合作。每年收集一套涵盖药物需求和药物供应措施的标准化指标的数据。此外,EMCDDA与欧洲刑警组织一起负责欧盟的新精神活性物质(NPS)预警系统。这一三步机制允许共享关于在欧洲出现的可能对健康构成类似于联合国公约管制药物风险的非受管制精神活性物质的信息。如果值得,提供给早期预警系统的信息可能触发由EMCDDA的科学委员会进行的风险评估。这项工作可能会导致在整个欧盟范围内引入快速通道控制措施的决定。在这篇社论中,我们考虑一个更加全球联合、充满活力和创新的药物市场如何影响药物供应和药物使用问题。在此过程中,我们以Dusunen Adam的评论和分析为基础精神病学和神经科学杂志2018;31:31 -237客座编辑/ Misafir编辑DOI: 10.5350/DAJPN20183103001
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