Local view for "http://purl.org/linkedpolitics/eu/plenary/2010-09-22-Speech-3-964"
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"en.20100922.20.3-964"2
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"Pharmacovigilance is the name of the system for monitoring the safety of medicinal products after they have been authorised. In order to be able to guarantee patients the best possible protection, information on Adverse Drug Reactions (ADRs) should be collated from the whole of the EU quickly and with no red tape. Only in this way can quick action be taken and an assessment of the follow up made. In addition, it would be of enormous benefit to patients if they could find out about ADRs from a central location. I voted in favour of the report, as its aim is for unbureaucratic and swift action to be taken in the area of pharmacovigilance."@en1
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