End of the CLP transitional period
The transitional period for the conversion to the new CLP (Classification, Labelling, Packaging) regulation (EC regulation no. 1272/2008) will end on 1 June 2015. “Companies that have not yet switched their product range to the labelling based on the CLP regulation should urgently become active now,” advises Jochen Dettke, expert in chemicals law at DEKRA. In a first step, the classification of the products has to be determined from the formulation in accordance with the rules of the CLP regulation. A simple conversion of the existing product classification based on the preparations directive is not advisable – it frequently leads to incorrect results. In some cases, additional laboratory tests also have to be carried out as even the underlying methods have changed.
The classification then produces the labelling with pictographs and signal words as well as the H (Hazards) and P (Precautions) phrases. This information is documented on the safety data sheet and the label. In the majority of cases, more pictographs are required based on the CLP regulation than before, with the result that it may be necessary to redesign the label. The packaging plant must therefore take into consideration in its planning the time frame for the production of new packaging.
The classification of the product may in some cases turn out to be stricter than before. For example, the irritant effect on the eyes will have to be seen more frequently on the label than before. Formulators should therefore check – if necessary with expert support – whether the classification as “corrosive” can be avoided by adjusting the formulation. The same applies for the acute toxicity classification.
DEKRA is providing support for importers and formulators in these tasks.
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