CLP的要求是什么?

CLP要求所有进口商, 厂家和下游用户进行分类, label and package substances and mixtures adequately before they can be placed on the market. 巴黎人官方网登录网址 can help to determine your 公司’s CLP requirements for chemical substances and mixtures within the EEA.

分类

The aim of classification is to ensure all substances and mixtures that feature hazardous properties are correctly identified. 为了遵守这一点, 公司 must determine the classification of substances and mixtures before they are placed on the market.

自我分类包括审查物理信息, 健康, 环境或其他危害, 并与CLP规例所订的准则进行比较. 许多普通物质都有统一的分类, 列于CLP附件六, 并且必须相应地分类, 至少.

巴黎人官方网登录网址’s team of regulatory and toxicological experts can help you to review information related to your substance or mixture and derive the classification.

标签

一旦物质或混合物被分类, 任何风险都需要有效地与客户沟通. 除了, 制造商 and importers of certain articles must communicate identified hazards to other actors in the supply chain. 这是通过标签来完成的, CLP定义标签的内容和各种标签元素的布局. 除了, t在这里 may be additional packaging requirements such as child-resistant fastenings or tactile warnings of danger (TWD).

巴黎人官方网登录网址可以帮助识别CLP法规要求的所有标签要求.

通知委员会&L库存

某些物质的进口商和制造商, mixtures and articles must submit a notification to the 分类 and 标签 Inventory within one month from them being placed on the market. 通知必须遵循特定格式，由进口商提交, 制造商, 仅限代表或第三方.

巴黎人官方网登录网址可以帮助创建通知并将其提交给C&L库存.

中毒中心通知

2017年，CLP法规增加了新的附件, which requires importers and downstream users to submit harmonised information on mixtures they place on the market which are classified for any 健康 or physical hazard. This information has to be submitted to the appointed bodies (the Poison Centres) in every Member State in which the mixture is sold, 并用于紧急卫生应对.

巴黎人官方网登录网址 can help you to prepare and submit the necessary notifications to Poison centres throughout the EEA.

安全数据表

Regulation (EC) No 1907/2006 (REACH) requires 安全数据表 (SDS) to be supplied to professional customers in order to convey CLP information about the substance or mixture. 在CLP下被分类为有害的物质或混合物需要sds, 或持续, 生物蓄积性和毒性(PBT)或非常持久和非常生物蓄积性(vPvB), 或者某种物质是否被列入REACH候选清单, 或者其他一些条件也适用. The SDS follows an internationally-agreed 16 section standard format and must be supplied in the official language of the Member State(s) w在这里 the substance or mixture is placed on the market, 除非有关成员国另有规定.

Importantly if a substance is manufactured or imported into the EEA at >10 tonnes/year and the substance is classified as hazardous under CLP, 应准备扩展的SDS (eSDS)并提供给客户. 这包含一个附加附件，其中包含一个或多个暴露场景。.

巴黎人官方网登录网址可以帮助准备符合clp的sds & esds.

CLH档案

根据欧盟农药或杀菌剂法规注册为活性物质的物质, 或CLP分类为致癌的物质, mutagenic or toxic to reproduction (CMR) require a CLH dossier be prepared and submitted to ECHA for evaluation. 利用现有的科学数据, CLH档案必须审查体检, 健康, environmental and other hazards of the substance to derive/justify the CLP classification/non-classification. CLH档案通常由成员国/主管当局提交, 但通常由物质注册人或供应商制备.

With extensive experience through our dedicated EU pesticide and biocide regulatory teams, 由技术专家和 化学Expertise， 巴黎人官方网登录网址可以协助准备和提交CLH档案.