Interview with Julie Power about the involvement and role of patient organizations in FAIRVASC project has been published.
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Within FAIRVASC Workpackage 2 (WP2) will capture the legal and ethical environment of each registry, patient perspectives on data sharing and re-use, […]
The FAIRVASC consortium held its second plenary meeting on 05 July 2021 (delivered online due to the COVID-19 Pandemic). Project partners from […]
The FAIRVASC consortium will meet for a Plenary meeting in the Conference Center at the Faculty of Medicine in Kraków, Poland on […]
We are happy to present an analysis of the data quality from the FAIRVASC registries. The Data Quality Team on behalf of […]