Data about people with CF who become infected with SARS-Cov-2 have been collected by CF patient registries throughout Europe.
The 20th Scientific Meeting hosted by the scientific board of the Mukoviszidose e.V. (FGM) will take place in September.
Topic: CF Registry: Ready for science!? - Value of registry data...Read more
We are appy to announce three webinars dedicated to Basic science.
We thank Carlos Farinha, Nicoletta Pedemonte and Jeffrey Brodsky for designing this series of webinars.
We are pleased to announce that the registration platform to the 44th European Cystic Fibrosis Conference, taking place on 9 - 12 June 2021, is now open!
More information...Read more
The Abstract Submission platform for the ECFS 2021 Conference is now open.
Abstract submission deadline: 22 January 2021
The ECFS Patient Registry Annual Data Report 2018 is available. Each calendar year the ECFS Patient Registry publishes a detailed Annual Report with demographic and clinical data from people with...Read more
The 2019 Annual Report of the CTN is now available in Dutch
The ECFS Standards of Care Project is inviting you to participate in the ECFS Standards of Care Twinning project. The Twinning project aims to build up a friendship and partnership...Read more
The ECFS Psychosocial Special Interest Group and the ECFS Mental Health Working will organise a webinar on
Tuesday 22 September 2020 - 13:00 - 17:00 CET
The course is an...Read more