Activities of Amalia SARTORI related to 2007/0121(COD)
Plenary speeches (2)
Classification, labelling and packaging of substances and mixtures - Classification, labelling and packaging of substances and mixtures (amendment of Directives 76/768/EEC, 88/378/EEC, 1999/13/EC, 2000/53/EC, 2002/96/EC and 2004/42/EC) - Classification, labelling and packaging of substances and mixtures (amendment of Regulation (EC) No 648/2004) (debate)
Classification, labelling and packaging of substances and mixtures - Classification, labelling and packaging of substances and mixtures (amendment of Directives 76/768/EEC, 88/378/EEC, 1999/13/EC, 2000/53/EC, 2002/96/EC and 2004/42/EC) - Classification, labelling and packaging of substances and mixtures (amendment of Regulation (EC) No 648/2004) (debate)
Reports (1)
REPORT Proposal for a regulation of the European Parliament and of the Council on classification, labelling and packaging of substances and mixtures, and amending Directive 67/548/EEC and Regulation (EC) No 1907/2006 PDF (591 KB) DOC (787 KB)
Amendments (5)
Amendment 53 #
Proposal for a regulation – amending act
Recital 26
Recital 26
(26) For the purpose of classification, data should not be generated by means of testing on non-humans and non-human primates primates. For the sole purpose of classification, the generation of data by means of testing on humans is generally not acceptable and should only be undertaken when no other alternatives are possible. Available, reliable epidemiological data and scientifically valid experience with regard to the effects of substances and mixtures on humans (e.g. occupational data and data from accident databases) should be taken into account and be given priority over data derived from animal studies when they demonstrate hazards not identified from those studies. Results of animal studies should be weighed againstcompared with results of data from humans and expert judgement should be used to ensure the best protection of human health when evaluating both the animal andand that the classification of the substance or mixture is in accordance with its actual effects on human datahealth.
Amendment 72 #
Proposal for a regulation – amending act
Article 7 - paragraph 2
Article 7 - paragraph 2
2. Tests on humans andfor the sole purpose of this Regulation are generally not acceptable and shall only be undertaken when no other alternatives are possible to ensure the best protection of human health and the classification of a substance or mixture according to its actual effects on human health. Tests on non-human primates shall not be performed for the purposes of this Regulation.
Amendment 118 #
Proposal for a regulation – amending act
Article 33 – paragraphs 1 and 2
Article 33 – paragraphs 1 and 2
The supplier of a substance or a mixture shall take all appropriate measures to update the label without delay following any change to the classification and labelling of the substance or mixture. The supplier of a mixture referred to in Article 24 shall upd, without delay and in any case not later the label without delay following anyan twelve months after the change to theof classification of the substance and the labelling of the mixture.
Amendment 120 #
Proposal for a regulation – amending act
Article 36a (new)
Article 36a (new)
Article 36a Labelling of detergents The labelling rules provided for in this Title shall be without prejudice to Regulation (EC) No 648/2004.
Amendment 126 #
Proposal for a regulation – amending act
Article 41 - paragraph 1 - introductory part
Article 41 - paragraph 1 - introductory part
1. Any manufacturer or importer, or group of manufacturers or importers, hereinafter “the notifiers”, who places on the market a substance subject to registration in accordance with Article 6(1) of Regulation (EC) No 1907/2006 in a quantity of one tonne or more per year or a substance that is classified as hazardous on its own or in a mixture above the concentration limits specified in Directive 1999/45/EC or in this Regulation, where relevant, which results in the classification of the mixture as hazardous, shall notify to the Agency the following information in order for it to be included in the inventory referred to in Article 43: