Hemophilia Federation of America

Hemophilia Federation of America (HFA) is a non-profit 501(c)3 organization incorporated in 1994 to address the evolving needs of the bleeding disorders community. We serve as a consumer advocate for safe, affordable, & obtainable blood products and health coverage, as well as a better quality of life for all persons with bleeding disorders. HFAs ongoing consumer advocacy agenda includes product safety, as well as accessibility, affordability, & availability of the products the individuals of this community require. Based in Washington, DC, HFA consists of a national office, organization, and 30+ community-based organizations made up of numerous parents, children, siblings, grandparents...

Public policy,bleeding disorders,hemophilia,blood,genetic disorders,medicine,hematology,von willebrand disease,coagulation,advocacy,health insurance,outreach,pharmaceuticals,special needs,pharmacy,government relations,biotechnology,education,health,and fitness

Hemophilia federation of america operates in the Public policy offices industry.

Hemophilia federation of america's revenue is 11m - 100m

Hemophilia federation of america has 11 - 50 employees.