Local view for "http://purl.org/linkedpolitics/eu/plenary/2012-06-14-Speech-4-330-500"

Predicate	Value (sorted: default)
rdf:type	lpv_eu:Speech2
dcterms:Date	"2012-06-14"^^xsd:date2
dcterms:Is Part Of	lp_eu:Explanations of vote2
dcterms:Language	"hu"^^xsd:language2
lpv:document identification number	"en.20120614.22.4-330-500"2
lpv:hasSubsequent	lp_eu:2012-06-14-Speech-4-330-4682
lpv:speaker	lp:Zoltán Bagó2
lpv:spokenAs	member; Delegation for relations with Japan (2010-10-06--2014-06-30)3 substitute; Delegation to the EU-Croatia Joint Parliamentary Committee (2010-09-28--2013-06-30)3 member; EPP (2010-09-12--2014-06-30)3 unknown; Fidesz-Magyar Polgári Szövetség-Keresztény Demokrata Néppárt (2010-09-12--2014-06-30)3 substitute; PETI (2012-01-19--2014-06-30)3 member; CULT (2012-01-19--2014-06-30)3
lpv:translated text	"− Defective silicone gel breast implants made by the French company PIP – I supported the motion for a resolution because the investigation launched against French manufacturer PIP (Poly Implant Prothèse) drew attention to the deficient transposition of European legislation on medical devices. Furthermore, the case highlighted the unsatisfactory functioning of the current system of certification of compliance with essential health and safety requirements. I agree that Member States should strengthen their cooperation and tighten controls in respect of medical devices in order to prevent similar cases from occurring. It would be important to know about Member State proceedings against various manufacturers, or whether the national authorities have banned or placed restrictions on their products. An ideal solution would be the creation of a single European database that would bring together information about the medical devices available on the market."@en1

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