Hemophilia Federation Of America
Public Policy, 820 1st St Ne, , District of Columbia, Washington, 20002, United States, 11-50 Employees
Phone Number: +12*********
Who is 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 ...
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Headquarters: 820 1st St Ne, Washington, District of Columbia, 20002, United States
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Date Founded: 1994
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Employees: 11-50
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Revenue: $25 Million to $50 Million
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Active Tech Stack: See technologies
Industry: Public Policy
SIC Code: 8322
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NAICS Code: 624190 |
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Frequently Asked Questions Regarding Hemophilia Federation of America
Answer: Hemophilia Federation of America's headquarters are located at 820 1st St Ne, , District of Columbia, Washington, 20002, United States
Answer: Hemophilia Federation of America's phone number is +12*********
Answer: Hemophilia Federation of America's official website is https://hemophiliafed.org
Answer: Hemophilia Federation of America's revenue is $25 Million to $50 Million
Answer: Hemophilia Federation of America's SIC: 8322
Answer: Hemophilia Federation of America's NAICS: 624190
Answer: Hemophilia Federation of America has 11-50 employees
Answer: Hemophilia Federation of America is in Public Policy
Answer: Hemophilia Federation of America contact info: Phone number: +12********* Website: https://hemophiliafed.org
Answer: 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 and friends impacted by a bleeding disorder. Many non-affected individuals and organizations such as healthcare providers, sponsors, donors, & specialty pharmacies play a significant role in the community. HFA utilizes its collaborative federation to strengthen community support and awareness, develop effective local organizations, and implement valuable community-based programs. These programs include a wide range of adult outreach initiatives, as well as broad-based support for families with bleeding disorders/hemophilia. HFA represents the bleeding disorders community on Capitol Hill, with the FDA, Centers for Disease Control and Prevention, and other key agencies. HFA strives to educate the community and provide tools that give the community a voice at state & federal legislatures.
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