Information for Professionals
European Reference Network for rare immune disorders
- RITA members are uniquely placed to harmonise diagnosis and therapy of affected patients across Europe, building a structure that will facilitate cross-fertilisation of knowledge, shared approaches to management and economies of scale across the three streams.
- RITA will reinforce research and epidemiological surveillance, develop quality and safety benchmarks and spread best practices exploiting innovations in medical science and health technologies.
- On its aim of helping Member States with an insufficient number of patients with a particular rare immune disorder, RITA will maximise the cost-effective use of resources facilitating mobility of expertise whenever the situation requires it.
How to join?
The first ERNs will be up and running in 2017. Further calls for new healthcare providers to join the existing networks will follow in 2018. Please check our FAQs this regarding or find out all information about the ERNs here.
Contact the RITA Secretariat: firstname.lastname@example.org