Historic Time in Treatment of CF as Promising Drugs Reach Phase 3 Trials
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Press Release
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Oct. 8, 2009
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4 min read
More than 4,600 cystic fibrosis researchers and health care professionals gathered Oct. 27 - 29 in Orlando for the 30th annual North American Cystic Fibrosis Conference. Recordings of the three plenary sessions are now available online.
Press Release
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Nov. 4, 2016
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4 min read
Medical Experts From 46 Countries to Collaborate at World's Largest Forum on CF Research and Care for Life-Threatening Genetic Disease
Press Release
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Oct. 26, 2017
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4 min read
These awards have been created to recognize and honor the contributions of those committed to care of individuals with cystic fibrosis and driving scientific advancements in CF research.
The CF Foundation 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 centers. Researchers also use the Patient Registry to study CF treatments and outcomes and to design CF clinical trials.