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serious adverse event

as defined in Directive 2002/98/EC of the European Parliament and of the Council of 27…, Article 3, point (g)

any untoward occurrence associated with the collection, testing, processing, storage and distribution, of blood and blood components that might lead to death or life-threatening, disabling or incapacitating conditions for patients or which results in, or prolongs, hospitalisation or morbidity

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