Local view for "http://purl.org/linkedpolitics/eu/plenary/2008-10-22-Speech-3-037"

Predicate	Value (sorted: default)
rdf:type	lpv_eu:Speech2
dcterms:Date	"2008-10-22"^^xsd:date2
dcterms:Is Part Of	lp_eu:Variations to the terms of marketing authorisations for medicinal products - Counterfeiting of medicinal products (debate)2
dcterms:Language	"it"^^xsd:language2
lpv:document identification number	"en.20081022.2.3-037"2
lpv:hasSubsequent	lp_eu:2008-10-22-Speech-3-0382
lpv:speaker	lp:Donato Tommaso Veraldi2
lpv:spokenAs	member; ALDE (2006-05-08--2009-07-13)3 unknown; Partito Democratico (2008-02-07--2009-07-13)3 substitute; ENVI (2008-05-14--2009-07-13)3 member; AGRI (2007-01-31--2009-07-13)3 member; Delegation for relations with Mercosur (2007-03-14--2009-07-13)3
lpv:translated text	"Mr President, ladies and gentlemen, thank you for the opportunity given to me to discuss the excellent work carried out by the rapporteur, Mrs Grossetête, and this proposal for a directive aimed at providing Community regulation applicable to all types of marketing authorisations for medicinal products. This is a positive directive, welcomed for its objectives of protecting public health and cutting red tape. The proposal for a directive is of a legal nature, introducing simple amendments to the legal basis behind the rules on variations, such as the introduction of a new therapeutic indication or a new method of administration, made to medicinal products for human or veterinary use after they are first placed on the market. Harmonisation in this area has become necessary, if not crucial, because without a single Community legal framework, variations concerning national authorisations will continue to be subject to national laws that differ from one Member State to another, as is the case at present."@en1
lpv:videoURI	<go to Events_and_structure europarl>2

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