


Hemophilia Federation of America
Hospitals and Health Care • Washington, District of Columbia, United States • 21-50 Employees
Company overview
| Headquarters | 999 N. Capitol Street NE, Suite 301, Washington, DC 20002, US |
| Phone number | +18002309797 |
| Website | |
| NAICS | 92 |
| SIC | 839 |
| Keywords | Public Policy, Biotechnology, Health Insurance, Education, Government Relations, Special Needs, Pharmaceuticals, Health, Outreach, Fitness, Advocacy, Hematology, Medicine, Pharmacy, Coagulation, Genetic Disorders, Blood, Bleeding Disorders, Hemophilia, Von Willebrand Disease |
| Founded | 1994 |
| Employees | 21-50 |
| Socials |
Key Contacts at Hemophilia Federation of America
Adam Alver
Policy Director
Ray Riordan
National Director Of Advocacy
Dan Kelsey
President And Chief Executive Officer
Marc Pangilinan
Director, Health Equity And Community Engagement
Matthew Landseadel
Director Of Technology Services
Lew Wyman-Collins
Board Of Directors; Medical Advisory Board
Jan Hamilton
Executive Director
Hemophilia Federation of America Email Formats
Hemophilia Federation of America uses 5 email formats. The most common is {first initial}.{last name} (e.g., j.doe@hemophiliafed.org), used 45.5% of the time.
| Format | Example | Percentage |
|---|---|---|
{first initial}.{last name} | j.doe@hemophiliafed.org | 45.5% |
{first name}.{last name} | john.doe@hemophiliafed.org | 31.8% |
{last name}.{last name} | doe.doe@hemophiliafed.org | 9.1% |
{first initial} | j@hemophiliafed.org | 4.5% |
{first name} | john@hemophiliafed.org | 4.5% |
About 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. HFA’s 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.
Hemophilia Federation of America revenue & valuation
| Annual revenue | $4,618,420 |
| Revenue per employee | $113,000 |
| Estimated valuation?This valuation is estimated based on industry average for the Hospitals and Health Care industry and current estimated revenues | $14,800,000 |
| Total funding | No funding |
Employees by Management Level
Total employees: 21-50
Seniority
Employees
Employees by Department
Hemophilia Federation of America has 6 employees across 4 departments.
Departments
Number of employees
Funding Data
Hemophilia Federation of America has never raised funding before.
Hemophilia Federation of America Tech Stack
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Frequently asked questions
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