Toolkit to Support Integration of European Reference Networks and National Healthcare Systems

April 2022

The European Reference Networks now have a clear governance structure for knowledge sharing and care coordination across the EU, but to benefit the 30 million people living with a rare disease in Europe, they must establish the operating mechanisms that will govern their interaction with national health systems. The integration of the ERNs and national health systems refers to the set of policies, rules and procedures required to anchor the ERN system to the national level so that all patients with a rare disease or complex condition across Europe can benefit from this model.

This toolkit is organised around 5 blocks of action at national level. For each area, the document collects the processes, tools, templates and best-practice examples to support the rare disease patient community engagement in the journey towards integrating ERNs into each national health system. These resources will need to be adapted to the local context through a structured dialogue with the rare disease community at national level, including national and regional health authorities, clinical leads, researchers, hospital managers, scientific societies, etc.  

The primary aim of this first edition of the ERN Integration Toolkit is to help the patient community engage with clinical teams, hospital managers and national/regional health authorities to take action towards integrating the ERNs into their national health systems. The Toolkit gathers a selection of existing methodologies, tools, templates and best practices that can be used to support implementation of the recommendations outlined in the ERN Board of Member States statement on integration of ERNs. The best practice examples have been developed based on a series of webinars on integration of ERNs organised by EURORDIS in 2021, during which ERN Board of Member State leads, ERN Coordinators and experts from the rare disease community were invited to present their best practices to the patient community.

Read the Toolkit

 
 
La voz de los pacientes de enfermedades raras en EuropaEURORDIS La voz internacional de las personas que tienen enfermedades rarasRare Disease International Reuniendo a pacientes, familiares y expertos para compartir experiencias en un foro moderado en distintos idiomas. RareConnect El Programa Rare Barometer es una iniciativa de EURORDIS que realiza encuestas para transformar las experiencias de los pacientes con enfermedades raras en cifras que puedan compartirse con los responsables políticos.Rare Barometer Una campaña internacional de sensibilización que se celebra todos los años el último día de febrero, El Día de las Enfermedades Raras es una iniciativa de EURORDISRare Disease Day Únete al mayor grupo de partes interesadas en toda Europa, en la Conferencia Europea sobre Enfermedades Raras y Medicamentos Huérfanos que se celebra cada dos años. ECRD es una iniciativa de EURORDISEuropean Conference on Rare Diseases