Aims of ENIRRI
To create a global database of patients with IRRIs in order to facilitate epidemiological and clinical research, and recruitment into clinical trials |
To attract new researchers into the IRRIs through presentations at the ERS International Congress, and dissemination of research priorities and knowledge |
To support and encourage early career researchers, many of who are applicants in this proposal, through multidisciplinary training opportunities and participation at senior levels in network activities |
To facilitate applications to industry and EU sources to build IRRI research capacity in Europe and beyond |
To build a network of experts in IRRI management who will determine the need for a task force, and the need for an IRRI consensus statement or guidelines for diagnosis, prevention and management |
EU: European Union.