Local view for "http://purl.org/linkedpolitics/eu/plenary/2010-11-24-Speech-3-206"

Predicate	Value (sorted: default)
rdf:type	lpv_eu:Speech2
dcterms:Date	"2010-11-24"^^xsd:date2
dcterms:Is Part Of	lp_eu:Explanations of vote2
dcterms:Language	"ro"^^xsd:language2
lpv:document identification number	"en.20101124.15.3-206"2
lpv:hasSubsequent	lp_eu:2010-11-24-Speech-3-2072
lpv:speaker	lp:Petru Constantin Luhan2
lpv:spokenAs	member; Delegation for relations with Switzerland and Norway and to the EU-Iceland Joint Parliamentary Committee and the European Economic Area (EEA) Joint Parliamentary Committee (2009-09-16--2014-06-30)3 substitute; LIBE (2009-07-16--2012-01-18)3 member; EPP (2009-07-14--2014-06-30)3 substitute; SEDE (2009-07-16--2012-01-18)3 unknown; Partidul Democrat-Liberal (2009-07-14--2014-06-30)3 member; REGI (2009-07-16--2012-01-18)3 substitute; Delegation for relations with Australia and New Zealand (2009-09-16--2011-12-19)3
lpv:translated text	"I voted in favour of this report as I am particularly interested in health-related topics, especially concerning equal access for patients to medical care and information. At the moment, the level of information about the medicines available on the market varies hugely in Europe, which I could say is even unfair to patients. Patients must have the right to obtain complete, correct information about medicines. The proposals from my colleague Christofer Fjellner have gone precisely in this direction, thereby giving priority to the patient. The amendments made by the European Parliament to the European Commission’s legislative proposal highlight that manufacturers of medicinal products must provide basic information such as product characteristics, a label, patient information leaflet and a publicly available version of the assessment report. However, so that we can ensure that the information is reliable, I think that national authorities must monitor stringently the specialist sites which supply such details."@en1

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