13 Amendments of Jean-François JALKH related to 2016/0130(COD)
Amendment 25 #
Proposal for a directive
Recital 1
Recital 1
(1) Directive 2004/37/EC aims to protect workers against risks to their health and safety from exposure to carcinogens or mutagens, mutagens or substances which may be toxic to reproduction at the workplace and lays down minimum requirements to that effect including limit values, on the basis of the available scientific and technical data.
Amendment 30 #
Proposal for a directive
Recital 2
Recital 2
(2) The limit values should be revised when necessary in the light of scientific data. The limit values should be revised systematically every two years in the light of modern, updated scientific data.
Amendment 34 #
Proposal for a directive
Recital 2 a (new)
Recital 2 a (new)
(2a) It should be borne in mind, nonetheless, that limit values protect workers only very partially; exposure times, both daily and over a career, even at very low rates, remain a preponderant factor.
Amendment 37 #
Proposal for a directive
Recital 2 b (new)
Recital 2 b (new)
(2b) It should also be borne in mind that the best protection, other than substitution, is still the equipment and training of workers.
Amendment 38 #
Proposal for a directive
Recital 3
Recital 3
(3) For some carcinogens and mutagens, mutagens or substances which may be toxic to reproduction, it is necessary to consider other absorption pathways, including the possibility of penetration through the skin, in order to ensure the best possible level of protection, and therefore to revise the exposure times and the protection equipment in the light of the minimum limit value indicated for each substance, where substitution is not possible.
Amendment 42 #
Proposal for a directive
Recital 3 a (new)
Recital 3 a (new)
(3a) It should be borne in mind that the dermal route is a major penetration pathway, which must de facto rule out the possibility of pregnant women manipulating carcinogens, mutagens and/or substances which may be toxic to reproduction.
Amendment 44 #
Proposal for a directive
Recital 4
Recital 4
(4) The Scientific Committee on Occupational Exposure Limits ( ‘the Committee’), comprising independent international experts from multiple sources, assists the Commission, in particular, in evaluating the latest available scientific data and in proposing occupational exposure limits for the protection of workers from chemical risks, to be set at EU level pursuant to Council Directive 98/24/EC47 and Directive 2004/37/EC. For the chemical agents o- toluidine and 2-nitropropane, there were no Committee recommendations available and other sources of scientific information, adequately robust and in the public domain, were considered 48 49. __________________ 47 Council Directive 98/24/EC of 7 April 1998 on the protection of the health and safety of workers from the risks related to chemical agents at work (fourteenth individual Directive within the meaning of Article 16(1) of Directive 89/391/EEC) (OJ L 131, 05.05.1998, p. 11). 48 http://monographs.iarc.fr/ENG/Monograph s/vol77/mono77- 11.pdfhttp://monographs.iarc.fr/ENG/Mon ographs/vol99/mono99-15.pdf et http://monographs.iarc.fr/ENG/Monograph s/vol100F/mono100F-11.pdf. 49 http://monographs.iarc.fr/ENG/Monograph s/vol1-42/mono29.pdf et http://monographs.iarc.fr/ENG/Monograph s/vol71/mono71-49.pdf.
Amendment 47 #
Proposal for a directive
Recital 5
Recital 5
(5) There is sufficient evidence of the carcinogenicity of respirable crystalline silica dust. On the basis of available information, including scientific and technical data, a limit value for respirable crystalline silica dust should be established. Respirable crystalline silica dust generated by a work process, with the exception of processes covered by the social dialogue on Workers’ Health Protection through the Good Handling and Use of Crystalline Silica and Products containing it49a, is not subject to classification in accordance with Regulation (EC) No 1272/2008 of the European Parliament and of the Council50. It is therefore appropriate to include work involving exposure to respirable crystalline silica dust generated by a work process in Annex I to Directive 2004/37/EC and to establish a limit value for respirable crystalline silica dust ('respirable fraction') . __________________, with a range of values from 0.1mg/m3 for quartz silica to 0.05mg/m3 for cristobalite. __________________ 49 a OJ C279, 17.11.2006, p.2-8 50 Regulation (EC) No 1272/2008 of the European Parliament and of the Council of 16 December 2008 on classification, labelling and packaging of substances and mixtures (OJ L 353, 31.12.2008, p. 1).
Amendment 50 #
Proposal for a directive
Recital 6
Recital 6
(6) Guides and good practice developed through initiatives by or peculiar to each Member State, such as the Social Dialogue "Agreement on Workers' Health Protection Through the Good Handling and Use of Crystalline Silica and Products Containing it" (NEPSi), are valuable and necessary instruments to complement regulatory measures and in particular to support the effective implementation of limit values.
Amendment 79 #
Proposal for a directive
Annex
Annex
Directive 2004/37/EC
Annex III – part A – column 4 – subcolumn mg/m3 – row 1
Annex III – part A – column 4 – subcolumn mg/m3 – row 1
Amendment 82 #
Proposal for a directive
Annex
Annex
Directive 2004/37/EC
Annex III – part A – column 4 – subcolumn mg/m3– row 2
Annex III – part A – column 4 – subcolumn mg/m3– row 2
0.02501
Amendment 85 #
Proposal for a directive
Annex
Annex
Directive 2004/37/EC
Annex III – part A – column 4 – subcolumn f/ml – row 3
Annex III – part A – column 4 – subcolumn f/ml – row 3
0.31
Amendment 94 #
Proposal for a directive
Annex
Annex
Directive 2004/37/EC
Annex III – part B
Annex III – part B
B. OTHER DIRECTLY RELATED PROVISIONS pm”Where good practices designed to reduce exposure to respirable crystalline silica (as defined in Annex I, point 6) are agreed by means of the social dialogue pursuant to Article 153(3) or Article 155(2) of the Treaty, including measures designed to enforce compliance with the limit value laid down in Section A above: implementation of these good practices shall make for full compliance with the Directive (2004/37/EC) on carcinogens and mutagens.