Hemophilia Council Of California
Public Policy, 358 5th Ave, Sacramento, California, 10001, United States, 1-10 Employees
Phone Number: +16*********
Who is HEMOPHILIA COUNCIL OF CALIFORNIA
Our Mission: To improve access to care and treatment options in order to advance the quality of life for people with bleeding disorders through advocacy, education, and outreach in collab...
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- Headquarters: 358 5th Ave, Sacramento, California, 10001, United States
- Employees: 1-10
- Revenue: $10 Million to $25 Million
Industry: Public Policy
SIC Code: 8322
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Frequently Asked Questions Regarding Hemophilia Council of California
Answer: Hemophilia Council of California's headquarters are located at 358 5th Ave, Sacramento, California, 10001, United States
Answer: Hemophilia Council of California's phone number is +16*********
Answer: Hemophilia Council of California's official website is https://hemophiliaca.org
Answer: Hemophilia Council of California's revenue is $10 Million to $25 Million
Answer: Hemophilia Council of California's SIC: 8322
Answer: Hemophilia Council of California has 1-10 employees
Answer: Hemophilia Council of California is in Public Policy
Answer: Hemophilia Council of California contact info: Phone number: +16********* Website: https://hemophiliaca.org
Answer: Our Mission: To improve access to care and treatment options in order to advance the quality of life for people with bleeding disorders through advocacy, education, and outreach in collaboration with its founding member organizations Our Vision: Open access to quality innovative care and choice of treatment for all people with bleeding disorders. Our History: The Hemophilia Council of California (HCC) was founded in 1982 by the four California hemophilia organizations and incorporated as a 501(c)(3) nonprofit public charity organization in 1989. Initially formed to coordinate state-level advocacy in response to HIV-contaminated clotting factor, the Council is now a consumer advocacy organization which coordinates statewide access, education, and advocacy efforts in conjunction with the four California bleeding disorders chapters. HCC advocates to protect access to care, promote progressive treatment options and advance the quality of life for individuals, families and caregivers living with hemophilia, von Willebrand disease and other bleeding disorders.
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