Workshop on haemophilia registries

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Date

Τετάρτη, 1 Ιούλιος 2015, Ολοήμερο

Τόπος

European Medicines Agency, Amsterdam, the Netherlands

Independent, disease-based registries are a potential source of valuable safety and efficacy data on products. The European Medicines Agency (EMA) is currently embarking on a strategy for patient registries. This initiative provides an appropriate starting point to consider what regulators need from haemophilia registries. The aim is to get the best capture of data in the European Union (EU) and build on existing expertise in this area. It is proposed to work with stakeholders on this topic, commencing with this EMA workshop. Places limited. Registration open until 01/06/2015.

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