Local view for "http://purl.org/linkedpolitics/eu/plenary/2010-11-24-Speech-3-954"

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	"it"^^xsd:language2
lpv:document identification number	"en.20101124.15.3-954"2
lpv:hasSubsequent	lp_eu:2010-11-24-Speech-3-2062
lpv:speaker	lp:Giovanni La Via2
lpv:spokenAs	member; Special committee on the policy challenges and budgetary resources for a sustainable European Union after 2013 (2010-06-17--2011-06-30)3 substitute; AGRI (2010-05-05--2012-01-18)3 member; BUDG (2010-05-05--2012-01-18)3 member; Delegation to the Euronest Parliamentary Assembly (2009-09-16--2014-06-30)3 member; EPP (2009-07-14--2013-05-21)3 unknown; Il Popolo della Libertà (2009-07-14--2013-12-15)3 member; Delegation to the EU-Moldova Parliamentary Cooperation Committee (2009-09-16--2014-06-30)3 substitute; Delegation for relations with Albania, Bosnia and Herzegovina, Serbia, Montenegro and Kosovo (2009-09-16--2013-06-12)3
lpv:translated text	"I congratulate Mr Fjellner on his important work as regards information to the general public on medicinal products for human use subject to medical prescription and more particularly on EU procedures for medicinal product authorisation and monitoring. The current EU legal framework on the scientific information provided to European consumers presents many problems, particularly as regards the different interpretations of the directive by individual Member States. The report approved today aims to improve the level of harmonisation of the regulations in the sector in an attempt to close the gaps and eliminate the disparities that exist today with regard to safeguarding the right to health. This is all situated within a broader strategy of health literacy, aimed at ensuring that the European public can, in fact, easily access scientific information on prescription-only medicines."@en1

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