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Author(s): Bruce Evatt,national patient registry
Format: Document
Having a national patient registry means being able to answer fundamental questions about the hemophilia population within a given country. This step-by-step guide outlines the basic principles of data collection, maintenance, and analysis and compares different types of registries.
The COVID-19 pandemic has significantly affected the bleeding disorders community, and many countries have seen their governments shift their focus
La pandémie de COVID-19 a beaucoup affecté la communauté des troubles de la coagulation, et beaucoup de pays ont vu
The COVID-19 pandemic has significantly affected the bleeding disorders community, and many countries have seen their governments shift their focus
Listen to this 1-hour webinar that took place on 27 November 2020, chaired by Baiba Zimele (WFH lay member). Presenters
Escuche este taller de 75 minutos que tuvo lugar el 26 de noviembre de 2020, moderado por Clive Smith (Reino
Listen to this 75-minute workshop that took place on 26th November 2020, moderated by Clive Smith (UK), WFH lay member,