CLP监管

CLP的要求是什么?

CLP需要所有的导入器, 制造商 and downstream users to classify, label and package substances and mixtures adequately before they can be placed on the market. TSG 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.

Self-classification involves reviewing information on the physical, 健康, 环境或其他危害, and comparing them with the criteria set out in the CLP监管. Many common substances have a harmonised classification, 列于中电附件VI, 并且必须相应地进行分类, 作为一个最低.

TSG’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

Once a substance or mixture has been classified, any risks need to be communicated to your customers effectively. 除了, 制造商 and importers of certain articles must communicate identified hazards to other actors in the supply chain. 这是通过标签来实现的, and CLP defines the content of a label and the layout of various label elements. 除了, t在这里 may be additional packaging requirements such as child-resistant fastenings or tactile warnings of danger (TWD).

TSG can help to identify all labelling requirements required by the CLP监管.

通知C&L库存

Importers and 制造商 of certain substances, 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. Notifications must follow a specific format and should be submitted by importers, 制造商, 仅代表或第三方.

TSG can help to create and submit notifications to the C&L库存.

毒药中心通知

A new Annex was added to the CLP 监管 in 2017, 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, and is used in an emergency 健康 response.

TSG can help you to prepare and submit the necessary notifications to Poison centres throughout the EEA.

安全数据表

监管 (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. SDSs are required for substances or mixtures classified as: hazardous under CLP, 或持续, bioaccumulative and toxic (PBT) or very persistent and very bioaccumulative (vPvB), or if a substance is included on the REACH candidate list, or if a number of other criteria apply. 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, unless the Member State(s) concerned provide(s) otherwise.

Importantly if a substance is manufactured or imported into the EEA at >10 tonnes/year and the substance is classified as hazardous under CLP, an extended SDS (eSDS) should be prepared and supplied to customers. This contains an additional annex with one or more exposure scenario(s).

TSG can help prepare CLP-compliant SDSs & esds.

CLH档案

Substances registered as active substances under EU pesticide or biocide regulations, or those classified under CLP as carcinogenic, 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, a CLH dossier must review the physical, 健康, environmental and other hazards of the substance to derive/justify the CLP classification/non-classification. A CLH dossier is normally submitted by the Member State/Competent Authority, but is often prepared by the substance registrant or supplier.

With extensive experience through our dedicated EU pesticide and biocide regulatory teams, 技术专家支持, TSG can assist preparing and submitting CLH档案.