Abstract
The European Cystic Fibrosis Society Patient Registry (Registry) contains data of over 50,000 patients from 40 countries. High quality data is essential for epidemiological research, pharmacovigilance studies and the annual reports.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Published version (
Free)
Free) 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
