Local view for "http://purl.org/linkedpolitics/eu/plenary/2010-09-22-Speech-3-218"

Predicate	Value (sorted: default)
rdf:type	lpv_eu:Speech2
dcterms:Date	"2010-09-22"^^xsd:date2
dcterms:Is Part Of	lp_eu:Explanations of vote2
dcterms:Language	"ro"^^xsd:language2
lpv:document identification number	"en.20100922.20.3-218"2
lpv:hasSubsequent	lp_eu:2010-09-22-Speech-3-2192
lpv:speaker	lp:Rovana Plumb2
lpv:spokenAs	member; EMPL (2009-07-16--2012-01-18)3 substitute; ENVI (2009-07-16--2012-01-18)3 substitute; Delegation to the Euronest Parliamentary Assembly (2010-05-04--2012-05-06)3 substitute; FEMM (2009-07-16--2012-01-18)3 unknown; Partidul Social Democrat (2009-07-14--2012-05-06)3 member; S&D (2009-07-14--2011-05-25)3 substitute; Delegation to the EU-Moldova Parliamentary Cooperation Committee (2009-09-16--2012-05-06)3 member; Delegation to the EU-Turkey Joint Parliamentary Committee (2009-09-16--2012-05-06)3
lpv:translated text	"The future regulation provides for a simplified procedure for product authorisation subject to certain conditions in order to avoid unnecessary costs and excessive fees. It is also a revision of the existing 1998 directive and establishes the focus of authorisation with the European Chemicals Agency. I support the gradual introduction of a centralised authorisation procedure: 2013 for low risk products and 2017 for all biocide types. The exclusion criteria for dangerous active substances (carcinogenic, mutagenic, toxic for reproduction, persistent, bio-accumulative) may be considered when a substitution plan for them is already available. Consequently, when a biocide containing an active substance which is a candidate for substitution is authorised, the time limit will be restricted to three years and there will have to be alternatives available which are not harmful to the environment or human health. The new regulation must take account of three essential areas: environmental protection, consumer protection and safe and practical implementation by manufacturers."@en1

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