-
HIT-CF program for rare mutations – August 2023 UpdateResubmission of the "Choices" clinical trial to CTIS, after its initial rejection, is... -
Bronze Healthcare Award 2023 for the Hellenic Cystic Fibrosis Association!The Hellenic Cystic Fibrosis Association was awarded with the Bronze Healthcare Award 2023...
-
Music event 40 years HCFA “Breath Unlimited- Be a life donor” with support of President of Hellenic Republic & Minister of HealthThe support messages of the President of Hellenic Republic and the Greek Minister...
-
CHMP positive opinion for Kaftrio/Kalydeco in CF children 2-5 y.o.European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) adopted...
-
Concert for Cystic Fibrosis “Breath Unlimited- Be a life donor”HCFA organises a live music event of free entry with the music band...
-
8th of September, Worldwide Cystic Fibrosis Day “Breath Unlimited – Be a life donor”"Unlimited Breath" is the claim of Cystic Fibrosis patients on this year's World...
-
Happy summer with Unlimited BreathThe Ηellenic Cystic Fibrosis Association wishes you a happy summer holiday full of...
-
Rare Barometer- Eurordis: survey on newborn screening for rare diseases until the 23rd of JulyUntil Sunday 23 July, the Rare Barometer survey of the European Rare Diseases...
-
July’s Online Coffee Break – Wednesday 19/7 at 20.00 pmDear members, We are pleased to welcome you to our last summer online...
-
Coordination of the President of our Association at the conference “Health financing: Challenges and solutions for a sustainable system”Moderator of the second session of the workshop "Health financing: Challenges and Solutions...
