A recent report of the joint action Towards the European Health Data Space (TEHDAS) examines EU-level and national funding for health data collection, access and use for secondary purposes, such as research. To ensure the economic sustainability of the forthcoming European health data space (EHDS), the EU and the member states will need to solve how…
A recent report of the joint action Towards the European Health Data Space (TEHDAS) identifies a minimum set of technical services – basic software items – required for the cross-border secondary use of health data in Europe. The secondary use of health data involves using health data, such as patient records, for research, decision-making, and…
The European Medicines Agency (EMA) is organising a joint EMA/HMA/TEHDAS Data Quality Framework for Medicines workshop as a virtual meeting on April 7th from 13.00 – 17.15 CET. This workshop seeks to engage stakeholders early in the drafting process of an EU Network data quality framework, to ensure a robust starting point, in line with their…
The Innovative Health Initiative (IHI) is organising a series of live sessions on Innovative Medicines Initiatives (IMI) Impact, where key actors will explore the challenges and demonstrate how IMI contributes by engaging IHI/IMI stakeholders in a broader discussion on IMI’s impact, with this webinar focused on IMI’s impact on SMEs in health data management &…
The Fondazione Gianni Benzi is organizing the XIV Foresight Training Course (FTC) on the theme of « The health emergency: Regulatory crash and future perspectives » as a virtual meeting that will take place on December 10th, 2021 from 11.20 – 18.30 CET. The agenda features the following sessions: Session 1 – How the European regulatory framework reacted to the COVID-19 emergency: Extraordinary…
The Chan Zuckerberg Initiative (CZI) has launched a Request for Information (RFI): Patient Registry Data Interoperability as part of the Rare As One project, aimed at mapping data interoperability challenges and support ideas that will make it easier for patient communities to share data with researchers, and for researchers to fully leverage patient voices in…
The European Health Data & Evidence Network (EHDEN) Consortium and the European Patients’ Forum (EPF) have jointly developed a free course to provide non-experts with the knowledge they need to better understand the importance of real world data, how it’s protected, and the vital role they can play in the healthcare ecosystem and health research.…
RWE4Decisions, a multi-stakeholder initiative commissioned by the Belgian National Institute of Health, is organising a webinar entitled “Delivering a Health Data Strategy for the European Reference Networks (ERNs): Developing a Shared Vision with All Stakeholders” to discuss what a co-created Health Data Strategy for the ERNs could look like. The webinar will take place on September 29, 2021 from 16.00…