Endo-ERN is focused on 8 main thematic groups (MTGs) which cover rare and/or complex endocrine conditions
Endo-ERN is a network of 100+ Reference Centres (RCs) in 28 EU member states that offers access to clinical experts for patients with rare endocrine conditions.
Endo-ERN is the network for rare endocrine conditions providing healthcare professionals with access to a variety of resources to support patient care.
If you work at a member institution this page will help with your Endo-ERN contributions.
Access to rare disease expertise without the need to travel is a core ERN objective. Our ePAGs contribute to all Endo-ERN activities.
European Reference Networks are virtual networks involving Reference Centres across Europe. They aim to tackle complex or rare diseases and conditions that require highly specialised treatment and a concentration of knowledge and resources.
ERN members have access to the Clinical Patient Management System. This system can be used to discuss complex patient cases through the means of consultation panels. In order to access the CPMS you need to create an account by completing the following steps (See “How to Request authorization CPMS” for further guidance):
Request CPMS authorization in SAAS
ERN members have access to the Collaborative platform. This platform can be used to store documents concerning your projects, save shared events, and to have discussions. It is restricted to ERN use only and is not to be used for the exchange of patient data.
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