Harmonization of Chemical Classification and Labeling in the EU: An Overview of the CLP Regulation and ComplyMarket's Solutions
The Classification, Labelling and Packaging Regulation (CLP) ((EC) No. 1272/2008) is based on the United Nations Globally Harmonized System (GHS). Its aim is to ensure a high level of protection of health and the environment and the free movement of substances, mixtures and articles. The CLP Regulation amended the Dangerous Substances Directive (67/548/EEC (DSD)), the Dangerous Preparations Directive (1999/45/EC (DPD)) and Regulation (EC) No 1907/2006 (REACH). Since 1 June 2015, the CLP Regulation has been the only legislation in force in the EU for the classification and labelling of substances and mixtures.
CLP specifies detailed criteria for the identification elements such as pictograms, signal words and standard statements on hazard, prevention, response, storage and disposal for each hazard class and category. It also establishes general packaging standards to ensure the safe supply of hazardous substances and mixtures. In addition to communicating hazards through labelling requirements, the CLP Regulation also forms the basis for many pieces of legislation on chemical risk management.
Due to the notification obligation under CLP, manufacturers and importers must submit information on the classification and labelling of the substances they place on the market to ECHA's Classification and Labelling Inventory.
With the inclusion of a new Annex VIII in the CLP Regulation in 2017, poison centres now have harmonised information requirements for Article 45 notifications. This information is transmitted to the notified bodies in the Member States and used for emergency health responses.
How ComplyMarket can help you:
- Our team has extensive experience in regulatory support of the CLP Directive.
- We offer ad-hoc consulting services to ensure that you ensure compliance with CLP and other relevant regulations.