Harmonization of Chemical Classification and Labeling in the EU: An Overview of CLP Regulation and ComplyMarket Solutions
The Classification, Labelling and Packaging (CLP) Regulation (EC) No 1272/2008) is based on the United Nations Global Harmonized System (GHS). Its objective is to ensure a high level of protection of health and the environment, as well as 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, CLP is the only legislation in force in the EU for the classification and labelling of substances and mixtures.
The CLP sets out detailed criteria for labelling elements, such as pictograms, signal words and standard statements for hazards, prevention, response, storage and disposal, for each hazard class and category. It also lays down general packaging rules to ensure the safe supply of hazardous substances and mixtures. In addition to hazard communication through labelling requirements, CLP is also the basis for many legislative provisions on chemical risk management.
The notification obligation under CLP requires manufacturers and importers to submit classification and labelling information for substances they are placing on the market to the C&L Inventory managed by ECHA.
With the addition of the New Annex VIII to the CLP Regulation in 2017, poison centres now have harmonised reporting requirements for notifications under Article 45. This information is sent to designated bodies in the Member State and is used for emergency health responses.
How ComplyMarket can help you:
- Our team has extensive experience providing regulatory support for the CLP directive.
- We offer ad-hoc consulting services to help you ensure compliance with CLP and other relevant regulations.