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The CF Patient Registry collects information on the health status of people with cystic fibrosis who receive care in CF Foundation-accredited care centers and agree to participate in the Registry. This information is used to create CF care guidelines, assist care teams providing care to individuals with CF and guide quality improvement initiatives at care … Read more/marsicolunginstitute/wp-content/uploads/sites/547/2017/12/cysticfibrosisfoundation2x.png