The Cystic Fibrosis Foundation recently submitted comments to the National Institutes of Health on improving racial equity, diversity, and inclusion in the biomedical research workforce.
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April 15, 2021
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2 min read
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Dec. 29, 2009
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2 min read
Nearly 200 teens from across the country -- nearly half living with cystic fibrosis -- participated in the Foundation's Virtual Teen Advocacy Day to advocate for the CF community.
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June 26, 2020
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3 min read
More than 200 advocates gathered on Capitol Hill during the Cystic Fibrosis Foundation's 14th Annual March on the Hill, championing antibiotic research and development and other policy needs on behalf of people with CF.
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March 2, 2020
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3 min read
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Aug. 13, 2009
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2 min read
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July 23, 2007
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1 min read