Local view for "http://purl.org/linkedpolitics/eu/plenary/2012-09-10-Speech-1-234-000"

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"en.20120910.29.1-234-000"2
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"Madam President, it is absolutely necessary that we should continue to monitor medicines after their marketing authorisation, the more so given that they are only trialled on a relatively small number of patients. New knowledge often only comes to light once the medicine in question is already on the market. Medicinal products that require additional monitoring or are subject to a post-authorisation safety study (PASS) should be labelled to that effect using a black symbol. In addition, doctors, patients and the authorities must be told in good time – meaning as soon as possible – when and why a medicinal product that had, up to then, been regarded as safe is withdrawn from the market. Clearly, we cannot allow a situation where investors in pharmaceutical companies are informed before doctors and pharmacists. Ultimately, the monitoring of medicinal products, as good as it is, only serves patients if it warns them in good time of a dangerous medicine."@en1
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