Local view for "http://purl.org/linkedpolitics/eu/plenary/2003-12-17-Speech-3-110"

Predicate	Value (sorted: default)
rdf:type	lpv_eu:Speech2
dcterms:Date	"2003-12-17"^^xsd:date2
dcterms:Is Part Of	lp_eu:Vote2
dcterms:Language	"pt"^^xsd:language2
lpv:document identification number	"en.20031217.4.3-110"2
lpv:hasSubsequent	lp_eu:2003-12-17-Speech-3-1112
lpv:speaker	lp:José Ribeiro E Castro2
lpv:spokenAs	member; Committee on Citizens' Freedoms and Rights, Justice and Home Affairs (2002-01-17--2004-07-19)3 member; UEN (1999-11-17--2004-07-19)3 substitute; AFCO (2002-01-17--2004-07-19)3 member; Members from the European Parliament to the Joint Parliamentary Assembly of the Agreement between the African, Caribbean and Pacific States and the European Union (ACP-EU) (2002-02-06--2004-07-19)3 unknown; Partido Popular (1999-11-17--2004-07-19)3
lpv:translated text	". I welcome the efforts that have been made to establish a Community code for veterinary medicines. Guaranteeing a high level of public health protection in the European Union necessarily requires general provisions to be adopted on placing these veterinary medicines on the market. There is unfortunately no shortage of reasons for greater vigilance to be required for products made available to healthcare professionals. Care over the precision and reliability of information on medicinal products is becoming increasingly important, due to greater consumer awareness. I therefore believe we would do very well to insist on a clearer separation between ‘information on medicinal products’ and the ‘advertising of medicinal products’. Lastly, I agree with the idea that reasonable timescales must be set for protecting the rights of pharmaceutical products, because this alone – on a reasonable basis, of course, which I believe has been achieved as a result of the European Parliament’s action – will ensure the ongoing interest of the sector’s industries in pursuing and even stepping up their study and technological research efforts to find new and improved products."@en1

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