jueves, 18 de julio de 2019

Statements on integration of European Reference Networks into the national health systems and cooperation with industry

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PATIENTS, ORGANISATIONS, SERVICES

https://ec.europa.eu/newsroom/sante/newsletter-specific-archive-issue.cfm?archtype=specific&newsletter_service_id=1431&newsletter_issue_id=16186&page=1&fullDate=Thu 07 Mar 2019&lang=default

Interviews with key players
Interview with Andrzej Rys, European Commission – DG SANTE
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Interview with Eve Parier, Hospital manager of St Louis, Lariboisière, Fernand Widal – France
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News from the ERN community
Two statements adopted on ERNs integration into the national health systems and cooperation with industry
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ERN hospital managers committed to strengthen collaboration to support the implementation of the ERNs
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Support for the setting-up of registries of patients affected by rare diseases available for all the ERNs
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Good practices and inspirational stories
How the ERNs are embedded in national rare disease policy: the French experience
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The Hungarian National Plan: improving the care of people living with rare diseases
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How to customise the CPMS to specific ERN needs: the example of ERN-EYE
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Solving the unsolved rare diseases: the Solve-RD project
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Electronic reporting tool to support monitoring activity of the ERNs: the case of “e-REC” implemented by Endo-ERN
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Clinical Practice Guidelines for rare diseases, how to gather and adapt existing (rare) expertise to improve effectiveness and quality of care: the experience of ERN ReCONNET
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Information to patients and health professionals: VASCERN’s Do’s and Don’ts Factsheets for rare vascular disease patients
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A “CPMS newsletter” to keep healthcare professionals informed about the latest developments: an initiative of eUROGEN
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Education and training for patients and health professionals: the experience of ERKNet
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An online expert advice service for patients affected by respiratory rare diseases: the EXABO initiative set up by ERN-LUNG
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Training healthcare professionals: the webinars organised by EURO-NMD
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“Patient journeys” to help patients share their experience with their diseases: the experience of ERN GENTURIS
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Improving the transition from paediatric to adult healthcare: a project carried out by MetabERN
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Mapping of activity and expertise to support work in the field of rare diseases: the case of Transplantchild

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