The objectives of this study are (i) to analyse the workability of certain provisions of Annex VIII to Regulation (EC) No 1272/2008 of the European Parliament and of the Council, on classification, labelling and packaging of substances and mixtures (Commission Regulation (EU) 2017/542, on harmonised information relating to emergency health response, hereinafter ‘Annex VIII’) in relation to certain industries with complex material inputs and supply chains; and (ii) to investigate and propose options to address the workability issues raised by some stakeholders if they are confirmed, without losing necessary information for appointed bodies/poison centres to perform their duties in accordance with Article 45 of the CLP Regulation.

Service contract for a study: the objectives of the study are (i) to analyse the workability of certain provisions of Annex VIII to Regulation (EC) No 1272/2008 of the European Parliament and of the Council, on classification, labelling and packaging of substances and mixtures (Commission Regulation (EU) 2017/542, on harmonised information relating to emergency health response, hereinafter ‘Annex VIII’) in relation to certain industries with complex material inputs and supply chains; and (ii) to investigate and propose options to address the workability issues raised by some stakeholders if they are confirmed, without losing necessary information for appointed bodies/poison centres to perform their duties in accordance with Article 45 of the CLP Regulation.