Insights

Growing Financial Base With a substantial revenue range of 50 to 100 million dollars, the Bleeding Disorders Council of California has significant financial resources, indicating potential for investments in innovative treatment solutions, educational programs, or advocacy initiatives.

Targeted Advocacy Network The organization's longstanding history since 1982 and its focus on advocacy, education, and outreach suggest a strong position within the healthcare and public policy sectors, providing opportunities to deliver specialized solutions for access to care and policy engagement.

Technology Integration Utilizing diverse digital tools like Google Analytics, Stripe, and media players indicates an openness to technology adoption, opening avenues for digital health solutions, secure payment processing, or data analytics platforms tailored to their needs.

Focused Patient Advocacy The organization’s mission to improve access and treatment options for people with bleeding disorders presents opportunities to partner on patient-centered technologies, educational content, or treatment management tools that align with their advocacy goals.

Niche Market Presence As a specialized non-profit in the public policy space with a relatively small staff, there is potential for scalable, high-impact solutions aimed at strengthening their outreach, streamlining operations, or expanding their advocacy capacity without large organizational overhaul.

Bleeding Disorders Council of California Tech Stack

Bleeding Disorders Council of California uses 8 technology products and services including Open Graph, oEmbed, Font Awesome, and more. Explore Bleeding Disorders Council of California's tech stack below.

Open Graph

Content Management System

oEmbed

Dev Tools

Font Awesome

Font Scripts

Isotope

Javascript Libraries

Stripe

Payment Processing

reCAPTCHA

Security

MediaElement.js

Video Players

Google Analytics

Web Analytics

Bleeding Disorders Council of California Email Formats	Example	Percentage
FLast@hemophiliaca.org	JDoe@hemophiliaca.org	50%
FLast@hemophiliaca.org	JDoe@hemophiliaca.org	50%

Bleeding Disorders Council of California Email Formats

Example

Percentage

FLast@hemophiliaca.org

JDoe@hemophiliaca.org

50%

FLast@hemophiliaca.org

JDoe@hemophiliaca.org

50%

Frequently Asked Questions

What is Bleeding Disorders Council of California's official website and social media links?

Bleeding Disorders Council of California's official website is hemophiliaca.org and has social profiles on LinkedIn.

What is Bleeding Disorders Council of California's SIC code NAICS code?

Bleeding Disorders Council of California's SIC code is 8399 - Social Services, Not Elsewhere Classified NAICS code is 921 - Executive, Legislative, and Other General Government Support.

How many employees does Bleeding Disorders Council of California have currently?

As of December 2025, Bleeding Disorders Council of California has approximately 8 employees across 1 continents, including North America. Key team members include President: M. W.Communications & Programs Manager: A. P.Board Member/Volunteer: R. M.. Explore Bleeding Disorders Council of California's employee directory with LeadIQ.

What industry does Bleeding Disorders Council of California belong to?

Bleeding Disorders Council of California operates in the Public Policy Offices industry.

What technology does Bleeding Disorders Council of California use?

Bleeding Disorders Council of California's tech stack includes Open GraphoEmbedFont AwesomeIsotopeStripereCAPTCHAMediaElement.jsGoogle Analytics.

What is Bleeding Disorders Council of California's email format?

Bleeding Disorders Council of California's email format typically follows the pattern of FLast@hemophiliaca.org. Find more Bleeding Disorders Council of California email formats with LeadIQ.

Bleeding Disorders Council of California

Public Policy OfficesCalifornia, United States2-10 Employees

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.

Insights

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