CLP/SGA

Harmonising Chemical Classification and Labelling in the EU: An Overview of the CLP Regulation and ComplyMarket's Solutions

The Classification, Labelling and Packaging (CLP) Regulation ((EC) No 1272/2008) is based on the United Nations’ Globally Harmonised System (GHS). Its purpose 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 classification and labelling of substances and mixtures.

CLP sets detailed criteria for the labelling elements such as pictograms, signal words, and standard statements for hazard, prevention, response, storage, and disposal, for every hazard class and category. It also sets general packaging standards to ensure the safe supply of hazardous substances and mixtures. In addition to the communication of hazards through labelling requirements, CLP is also the basis for many legislative provisions on the risk management of chemicals.

The notification obligation under CLP requires manufacturers and importers to submit classification and labelling information for the substances they are placing on the market to the C&L Inventory held by ECHA.

With a new Annex VIII added to the CLP Regulation in 2017, poison centres now have harmonised information requirements for notifications under Article 45. This information is submitted to the appointed bodies in the Member State and is used for emergency health response.

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.