指令(EU) 2018/851下的SCIP数据库

Tim Becker
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摘要

随着即将推出的关于物品或复杂物体(产品)中所关注物质的数据库(以下简称SCIP数据库)1,欧盟的共同立法者已经为欧盟、国家和全球层面的所有相关方引入了一个雄心勃勃的项目。该要求载于关于废物的指令2008/98/EC第9(1)(i)和(2)条,并经欧洲议会和理事会2018年5月30日指令(EU) 2018/851(以下简称废物框架指令,WFD或修订的WFD)修订。在最近的SCIP研讨会20192上,欧洲化学品管理局(ECHA)与来自行业、当局和非政府组织的众多参与者介绍并讨论了ECHA应在2020年1月5日前建立的数据库的现状。特别是,ECHA对SCIP通知的详细信息要求的范围被业界批评为超出了法律界限,而其他人则支持ECHA的计划。这个问题具有高度的实际意义。从本质上讲,关键问题是行业是否可以依赖根据法规(EC) No 1907/2006 (REACH)第33(1)条已经传达的现有系统和数据,或者是否必须从通常漫长而复杂的全球供应链中收集额外的数据以进行SCIP通知,这些通知将于2021年1月5日到期。在此背景下,本文旨在深入研究新SCIP条款的法律背景,并基于欧盟委员会(EC)的基本原理,从法律角度讨论ECHA的详细信息要求。我们将看到,在欧盟法律中,对于颁布条款的解释,复述的作用是在此背景下提出的关键法律问题之一。
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The SCIP Database under Directive (EU) 2018/851
With the forthcoming database on substances of concern in articles as such or in complex objects (products) (hereafter SCIP database)1 the EU’s co-legislators have introduced a highly ambitious project for all parties involved at the EU, national and global level. The requirement is set out in Article 9(1)(i) and (2) of Directive 2008/98/EC on waste, as revised by Directive (EU) 2018/851 of the European Parliament and of the Council of 30 May 2018 (hereafter Waste Framework Directive, WFD or revised WFD). At its recent SCIP workshop 20192the EuropeanChemicals Agency (ECHA) presented and discussedwith numerous participants from industry, authorities and NGOs the current state of play of the database, which ECHA should establish by 5 January 2020. In particular, the scope of ECHA’s detailed information requirements for SCIP notifications was criticized from the industry side for exceeding legal boundaries, while others argued in support of the ECHA plans. This question is of high practical relevance. Essentially, the issue at stake is whether industry can rely on existing systems and data already communicated under Article 33(1) of Regulation (EC) No 1907/2006 (REACH), or whether additional data has to be collected from often long and complex global supply chains for the purpose of SCIP notifications, which are due as from 5 January 2021. Against this background, the present article aims to take a closer look at the legal background for the new SCIP provisions and discuss ECHA’s detailed information requirements from a legal point of view, based on the underlying rationale of the European Commission (EC). We will see that the role of recitals in EU law for the interpretation of enacting terms is one of the key legal issues raised in this context.
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