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分类与标签目录:ECHA 的作用与通报要求。

Classification & Labelling Inventory: role of ECHA and notification requirements.

机构信息

European Chemicals Agency, ECHA, Helsinki.

出版信息

Ann Ist Super Sanita. 2011;47(2):140-5. doi: 10.4415/ANN_11_02_04.

Abstract

The CLP Regulation introduces the criteria of the UN Globally Harmonised System of Classification and Labelling (UN GHS) in the EU. The European Chemicals Agency (ECHA) manages the CLP related tasks - such as harmonised classification and labelling, handling requests for alternative names and maintaining the Classification & Labelling Inventory (C&L) - to ensure consistent implementation in the EU. The obligations for industry depend on their role in the supply chain. Manufacturers and importers have to notify to ECHA the identity and classification and labelling of substances within one month of placing them on the market either on their own or in a mixture, and regardless of the quantitity. As of 3 January 2011 ECHA has received some 3.1 million notifications of over 107 000 substances. This information is stored in the C&L Inventory and accessible to Member State Competent Authorities. The non-confidential information will be made publicly available on ECHA's website in 2011.

摘要

《欧盟 CLP 法规》在欧盟采用了联合国全球化学品统一分类和标签制度(简称“UN GHS”)的标准。欧洲化学品管理局(ECHA)负责 CLP 相关任务,如协调分类和标签、处理替代名称的请求以及维护分类和标签登记册(简称“C&L 登记册”),以确保在欧盟内的统一执行。各行业的义务取决于其在供应链中的角色。制造商和进口商必须在将物质投放市场后一个月内,无论数量多少,将其自身或混合物中的物质的身份、分类和标签通知 ECHA。截至 2011 年 1 月 3 日,ECHA 已经收到了约 310 万份通知,涉及超过 10.7 万种物质。这些信息存储在 C&L 登记册中,供成员国主管当局使用。非机密信息将在 2011 年在 ECHA 的网站上公开提供。

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