EU CLP Compliance

The United Nations developed a Globally Harmonized System for the Classification and Labelling of Chemicals, known as GHS. As an international agreement, GHS is non-legally binding in Europe, therefore the GHS criteria was introduced into Europe via CLP.

EU CLP stands for the Regulation (EC) No 1272/2008 – classification, labelling and packaging of substances and mixtures (CLP). CLP introduces the United Nations globally harmonized system (UN GHS) for classification and labeling of chemicals into Europe. CLP entered into force on January 20, 2009.

On March 31, 2023, European Commission has released the amendments to the Annex I to Regulation (EC) No 1272/2008 as regards hazard classes and criteria for the classification, labelling and packaging of substances and mixtures (CLP), introducing several new classification criteria to identify endocrine disrupting chemicals (EDCs) and persistent and mobile substances.

The Transitional Period of CLP Regulation

The CLP Regulation replaced the Dangerous Substances Directive 67/548/EEC (DSD) and Dangerous Preparations Directive 1999/45/EC (DPD) in a stepwise approach during a transitional period. After June 1, 2015, both substances and mixtures have only been classified according to CLP.

How to Comply with CLP Regulation

The CLP Regulation, Article 46, on Enforcement and Reporting, states that “Member States shall take all necessary measures, including maintaining a system of official controls, to ensure that substances and mixtures are not placed on the market, unless they have been classified, labelled, notified and packaged in accordance with this Regulation”.

Generally speaking, companies shall classify substances or mixtures, submit C&L notifications to ECHA, and label and package their products in accordance with the CLP regulation. A CLP-compliant Safety Data Sheet containing the CLP classification and label must also be prepared and communicated to downstream users.

Our Service

• Re-classification and re-labeling of your substances or mixtures;

• Preparation of CLP-compliant labels;

• Notification to the Classification & Labeling Inventory (C&L notification);

• Preparation of Safety Data Sheets in accordance with CLP in member state languages;