Care-for-Rare Alliance

The Care-for-Rare Alliance is a Europe-wide open grant program that connects an international network of pediatricians and scientists in research & innovation, healthcare, as well as education and training. Its goal is the joint development of novel diagnostic and therapeutic concepts for rare diseases, particularly genetically caused immunodeficiencies. Through cross-border collaborations, research stays, workshops, and strategic meetings are initiated to strengthen young scientific talent and promote the mobility of young clinically active researchers. Additionally, travel grants for conferences are awarded and important IT infrastructures (e.g., Beacon, Sample Tracking System) are established to advance data exchange and variant analysis. With a focus on awareness, healthcare professionals as well as the general public are informed about the current state of research and sensitized to the topic of rare diseases.

Eligible for funding are educational institutions, public institutions, and private individuals engaged in research activities in the field of rare diseases who are employed at pediatric clinics or scientific institutes. Evaluation is based on professional expertise, the quality of the project, and the potential for international collaboration. Applications must include a CV and a detailed project or research description. Applications can be submitted at any time, as funding is awarded continuously. The Care-for-Rare Foundation thus not only supports the development of individual therapeutic approaches but also makes a significant contribution to the training of future generations of physicians and researchers. This program promotes scientific exchange at the highest level and paves the way for personalized medicine for affected children throughout the EU.