Developer docs
API playgroundTry for free, no card

Search company profiles

Hemophilia Foundation Southern California

Full company profile

uuid004keh1

Namestring
Hemophilia Foundation Southern California
Legal namestring
Hemophilia Foundation of Southern California
Websiteurl
hemosocal.org
Company typeenum
Private
Founded yearint
1954
Descriptiontext

The Hemophilia Foundation Southern California is a 501(c)(3) nonprofit founded in 1954 and headquartered in Pasadena, California, dedicated to serving individuals and families affected by hemophilia, von Willebrand disease, and other inherited bleeding disorders across nine Southern California counties. Its core service offerings include community education, advocacy on access and reimbursement issues, emergency financial assistance (including disaster-relief response such as wildfire support), scholarships, and recurring community programs including family retreats, the annual Familia de Sangre Spanish-language gathering, and industry-sponsored conferences.

The foundation operates a donor- and grant-funded nonprofit business model, generating revenue through pharmaceutical manufacturer sponsorships (Sanofi, Takeda, Genentech, Octapharma, Amgen), national advocacy coalition partnerships (NBDF, HFA, EveryLife Foundation, NORD), retail-cause partnerships (Kendra Scott), and individual donations. It does not sell products or services in a commercial sense. Its "technology stack" is conventional nonprofit infrastructure (events, scholarship administration, peer support) with no disclosed digital platforms or AI/ML components.

The organization is led by Executive Director Rigo Garcia (appointed July 2022) and Board President Rick Kelly, with 11-50 employees. Strategic priorities under current leadership include expanding rare-disease coalition engagement (Amgen/EveryLife #RAREis Scholarship Fund), federal regulatory advocacy on Medicaid/Medicare data privacy, and broadening the funding base through consumer-cause partnerships.

Short descriptiontext

The Hemophilia Foundation Southern California is a Pasadena-based 501(c)(3) nonprofit founded in 1954 that serves individuals and families affected by bleeding disorders across nine Southern California counties through education, advocacy, emergency financial assistance, scholarships, and community programs.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersPasadena, CA, United States
HQ citystring
Pasadena, CA
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
bleeding disorders support, patient advocacy services, community health education, emergency financial assistance, nonprofit healthcare foundation
Industry3 codes
1Disease-Specific Research & Support (e.g., Cancer, Diabetes, ALS)
CodeBPAGACAAPrimaryYes
2Health Promotion & Public Health Education (Community Workshops)
CodeEDAAAFAGPrimaryNo
3Public Health & Health Equity Organizations
CodeBPAGACALPrimaryNo
NAICS code4 codes
  • Voluntary Health Organizations813212
  • Individual and Family Services6241
  • Grantmaking and Giving Services81321
  • Religious, Grantmaking, Civic, Professional, and Similar Organizations813
SIC code4 codes
  • Services-Misc Health & Allied Services, Nec8090
  • Services-Social Services8300
  • Services-Membership Organizations8600
  • Services-Health Services8000
Product category
Patient Advocacy and Community Health Services
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model3 records
1Donations and Fundraising
TypeAffiliate Referral
Description

The foundation relies on charitable donations from individuals, corporations, and community members to fund programs, scholarships, and emergency assistance. Annual giving campaigns include Giving Tuesday and ongoing fundraising efforts.

hemosocal.org
2Event-Based Fundraising
TypeAffiliate Referral
Description

Partnership fundraising through events like Kendra Scott Shop for Good where 20% of sales are donated, and the annual Unite for Bleeding Disorders Walk to support scholarship programs.

hemosocal.org
3Emergency Financial Assistance Program
TypeOthers
Description

Provides temporary financial relief to families facing crisis for needs such as housing, transportation, food, and utility bills, funded through donations and fundraising.

hemosocal.org
Marketing channels6 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels3 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components4 values
Personnel, Operations, Marketing or Sales, Others
GTM typeB2C
B2C
Offering typeServices
Services
Core offering1 text field

The Hemophilia Foundation of Southern California is a 501(c)(3) nonprofit patient advocacy foundation that delivers free education, advocacy, support services, scholarships, and emergency financial assistance to individuals and families affected by inherited bleeding disorders (hemophilia A, hemophilia B, von Willebrand disease, inhibitors, rare factor deficiencies, platelet disorders). It runs annual educational conferences and family retreats, funds scholarships, distributes medical alert IDs, and provides emergency relief across nine Southern California counties.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 2 values shown
  • Over $115,000 in scholarship funds awarded during last decade
+1 more record
Product overview1 text field

Hemophilia Foundation of Southern California is a non-profit organization (founded in 1954) that serves as the leading resource for those affected by bleeding disorders in Southern California. The organization offers a portfolio of community support programs including education, advocacy, support services, scholarships, and emergency financial assistance. Its programmatic offerings include educational conferences (Family Information Day, Bleeding Disorders Conference, Familia de Sangre), family retreats (Hemochella, Women's Retreat, Men's Retreat), and an annual Back to School Event. Additional services include a Medical Alert ID Program, Community Groups, and a monthly Newsletter Subscription. The organization operates across 9 counties: Kern, Los Angeles, Ventura, Santa Barbara, San Luis Obispo, Orange, Riverside, San Bernardino, and Inyo.

Product and service14 records
1Education Programs
CategoryEducation and Community Programs
Description

Programs, conferences, workshops and events designed to increase awareness and share knowledge about bleeding disorders with patients, families, and medical professionals in Southern California.

2Advocacy Services
CategoryAdvocacy
Description

Advocacy on behalf of the bleeding disorders community to amplify their voice on policy, healthcare access, and related matters, delivered in partnership with NBDF and HFA at the national level.

3Scholarship Program
CategoryScholarships and Educational Financial Support
Description

Multi-scholarship program (Christopher Mark Pitkin Memorial, Joshua Kim Advocacy is in Your Blood, Victoria Mendoza Perez Healthcare) awarding funds to members of the bleeding disorders community pursuing education. Over $115,000 awarded during the last decade.

4Emergency Financial Assistance (EFA) Program
CategoryEmergency Financial Assistance
Description

Temporary financial relief for families in crisis, covering housing, transportation, food, and utility bills for individuals and families affected by bleeding disorders in Southern California.

5Medical Alert ID Program
CategoryPatient Safety Services
Description

Distributes medical alert identification tools to individuals with bleeding disorders to support their safety and emergency care.

6Family Information Day
CategoryCommunity Events
Description

Annual educational event bringing together families affected by bleeding disorders for information sharing and networking.

7Family Retreat (Hemochella)
CategoryCommunity Events
Description

Annual family retreat offering opportunities for families facing bleeding disorders to create memories and strengthen community connections. The 2023 'Hemochella' event drew 33 families (114 attendees).

8Women's Retreat
CategoryCommunity Events
Description

Annual retreat specifically for women affected by bleeding disorders, providing education and community support. The 2024 Women's Retreat drew 90 women.

9Men's Retreat
CategoryCommunity Events
Description

Event for boys, men, or those who identify as male with a bleeding disorder, or who are male parents, caregivers, spouses, or siblings of someone with a bleeding disorder.

10Familia de Sangre Conference
CategoryCommunity Events
Description

Annual Spanish-language conference for the bleeding disorders community, described as the country's largest Spanish-speaking conference for bleeding disorders.

11Bleeding Disorders Conference
CategoryCommunity Events
Description

Annual conference organized by the National Bleeding Disorders Foundation (NBDF) that HFSC participates in and promotes to Southern California community members.

12Back to School Event
CategoryCommunity Events
Description

Annual event helping families of children with bleeding disorders navigate returning to the classroom, including understanding educational rights (IEP/504 plans) and creating individualized health and academic plans.

13Community Groups
CategoryCommunity Support
Description

Facilitated community groups connecting individuals and families affected by bleeding disorders in Southern California.

14Monthly Newsletter Subscription
CategoryCommunication Services
Description

Monthly newsletter delivered online or by mail to subscribers, providing news, events, and updates for the bleeding disorders community.

Scale indicator5 records

Each record includes

Type, Value, Description, Source

Partnership11 partners
Strategic tierMajorTypeStrategic or Co-development PartnerAnnounced on2025-08-06
Description

HFA is a national organization representing the bleeding disorders community. HFSC partners with HFA on advocacy, education, and policy issues affecting patients including Medicaid/Medicare data privacy concerns.

Strategic tierImportantTypeGTM or Marketing PartnerAnnounced on2025-02-03
Description

Shop for Good partnership where 20% of purchases during designated periods support HFSC programs including Wildfire Relief Fund, Emergency Financial Assistance program, Medical Alert ID program, and educational scholarships.

Strategic tierImportantTypeGTM or Marketing PartnerAnnounced on2025-02-03
Description

Partners with HFSC to promote the #RAREis Scholarship Fund providing $5,000 scholarships to 104 rare disease recipients in 2025.

Strategic tierMajorTypeStrategic or Co-development PartnerAnnounced on2024-06-05
Description

NBDF is a national organization working to bleeding disorders community. HFSC works in partnership with NBDF on conferences, advocacy efforts, and policy initiatives at the national level.

Strategic tierCoreTypeGTM or Marketing PartnerAnnounced on2023-06-09
Description

Platinum sponsor of HFSC 2023 Family Retreat 'Hemochella'. Sanofi is a pharmaceutical company developing treatments for bleeding disorders.

Strategic tierCoreTypeGTM or Marketing PartnerAnnounced on2023-06-09
Description

Platinum sponsor of HFSC 2023 Family Retreat 'Hemochella'. Takeda is a pharmaceutical company developing treatments for bleeding disorders.

Strategic tierImportantTypeGTM or Marketing PartnerAnnounced on2023-06-09
Description

Gold sponsor of HFSC 2023 Family Retreat 'Hemochella'. Genentech develops treatments for rare diseases including bleeding disorders.

Strategic tierCoreTypeGTM or Marketing PartnerAnnounced on2023-06-09
Description

Gold sponsor of HFSC 2023 Family Retreat 'Hemochella'. HFA is a national advocacy organization for the bleeding disorders community.

Strategic tierImportantTypeGTM or Marketing PartnerAnnounced on2023-06-09
Description

Silver sponsor of HFSC 2023 Family Retreat 'Hemochella'. Octapharma develops and produces human proteins for bleeding disorders treatments.

Strategic tierNotableTypeStrategic or Co-development PartnerAnnounced on2022-07-28
Description

Former employer of current Executive Director Rigo Garcia, who served as Director of Health Education providing healthcare access to underserved communities.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2021-07-08
Description

HFSC participates in the HTC Western States Regional conference to discuss best practices and care for the bleeding disorders community. Supports HTC sustainability.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight4 records

Each record includes

Type, Description

Market position
Competitive moat3 records

Each record includes

Type, Details

Key risks5 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers2 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment4 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile2 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
No
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles5 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Hemophilia Foundation Southern California

Patient Advocacy and Community Health Serviceshemosocal.org

The Hemophilia Foundation Southern California is a Pasadena-based 501(c)(3) nonprofit founded in 1954 that serves individuals and families affected by bleeding disorders across nine Southern California counties through education, advocacy, emergency financial assistance, scholarships, and community programs.

What Hemophilia Foundation Southern California does

The Hemophilia Foundation Southern California is a 501(c)(3) nonprofit founded in 1954 and headquartered in Pasadena, California, dedicated to serving individuals and families affected by hemophilia, von Willebrand disease, and other inherited bleeding disorders across nine Southern California counties. Its core service offerings include community education, advocacy on access and reimbursement issues, emergency financial assistance (including disaster-relief response such as wildfire support), scholarships, and recurring community programs including family retreats, the annual Familia de Sangre Spanish-language gathering, and industry-sponsored conferences.

The foundation operates a donor- and grant-funded nonprofit business model, generating revenue through pharmaceutical manufacturer sponsorships (Sanofi, Takeda, Genentech, Octapharma, Amgen), national advocacy coalition partnerships (NBDF, HFA, EveryLife Foundation, NORD), retail-cause partnerships (Kendra Scott), and individual donations. It does not sell products or services in a commercial sense. Its "technology stack" is conventional nonprofit infrastructure (events, scholarship administration, peer support) with no disclosed digital platforms or AI/ML components.

The organization is led by Executive Director Rigo Garcia (appointed July 2022) and Board President Rick Kelly, with 11-50 employees. Strategic priorities under current leadership include expanding rare-disease coalition engagement (Amgen/EveryLife #RAREis Scholarship Fund), federal regulatory advocacy on Medicaid/Medicare data privacy, and broadening the funding base through consumer-cause partnerships.

Hemophilia Foundation Southern California firmographics

Firmographics
Name
Hemophilia Foundation Southern California
Legal name
Hemophilia Foundation of Southern California
Website
https://hemosocal.org
Company type
Private
Founded year
1954
Operating status
Operating
Headcount range
11–50 employees
Short description
The Hemophilia Foundation Southern California is a Pasadena-based 501(c)(3) nonprofit founded in 1954 that serves individuals and families affected by bleeding disorders across nine Southern California counties through education, advocacy, emergency financial assistance, scholarships, and community programs.
Ownership category
akta.pro rank

Hemophilia Foundation Southern California industry classification

Industry
Product category
Patient Advocacy and Community Health Services
NAICS
Voluntary Health Organizations (813212), Individual and Family Services (6241), Grantmaking and Giving Services (81321), Religious, Grantmaking, Civic, Professional, and Similar Organizations (813)
SIC
Services-Misc Health & Allied Services, Nec (8090), Services-Social Services (8300), Services-Membership Organizations (8600), Services-Health Services (8000)
akta.pro primary industry
Disease-Specific Research & Support (e.g., Cancer, Diabetes, ALS) (BPAGACAA)
akta.pro secondary industries
Health Promotion & Public Health Education (Community Workshops) (EDAAAFAG), Public Health & Health Equity Organizations (BPAGACAL)

Keywords

  • Bleeding disorders support
  • Patient advocacy services
  • Community health education
  • Emergency financial assistance
  • Nonprofit healthcare foundation

Where Hemophilia Foundation Southern California is headquartered

Location

Headquarters

HQ city
Pasadena, CA
HQ country
United States
HQ region
North America

Offices1 record

Markets served

Hemophilia Foundation Southern California business model

Business model
GTM type
B2C
Offering type
Services
Cost components
Personnel, Operations, Marketing or Sales, Others

Revenue model

  1. Donations and Fundraising: The foundation relies on charitable donations from individuals, corporations, and community members to fund programs, scholarships, and emergency assistance. Annual giving campaigns include Giving Tuesday and ongoing fundraising efforts.
  2. Event-Based Fundraising: Partnership fundraising through events like Kendra Scott Shop for Good where 20% of sales are donated, and the annual Unite for Bleeding Disorders Walk to support scholarship programs.
  3. Emergency Financial Assistance Program: Provides temporary financial relief to families facing crisis for needs such as housing, transportation, food, and utility bills, funded through donations and fundraising.

Go-to-market motion2 records

Distribution channels3 records

Marketing channels6 records

Hemophilia Foundation Southern California product offering

Product offering

Core offering

The Hemophilia Foundation of Southern California is a 501(c)(3) nonprofit patient advocacy foundation that delivers free education, advocacy, support services, scholarships, and emergency financial assistance to individuals and families affected by inherited bleeding disorders (hemophilia A, hemophilia B, von Willebrand disease, inhibitors, rare factor deficiencies, platelet disorders). It runs annual educational conferences and family retreats, funds scholarships, distributes medical alert IDs, and provides emergency relief across nine Southern California counties.

Product overview

Hemophilia Foundation of Southern California is a non-profit organization (founded in 1954) that serves as the leading resource for those affected by bleeding disorders in Southern California. The organization offers a portfolio of community support programs including education, advocacy, support services, scholarships, and emergency financial assistance. Its programmatic offerings include educational conferences (Family Information Day, Bleeding Disorders Conference, Familia de Sangre), family retreats (Hemochella, Women's Retreat, Men's Retreat), and an annual Back to School Event. Additional services include a Medical Alert ID Program, Community Groups, and a monthly Newsletter Subscription. The organization operates across 9 counties: Kern, Los Angeles, Ventura, Santa Barbara, San Luis Obispo, Orange, Riverside, San Bernardino, and Inyo.

Differentiator

Problem solved

Functional benefit

Products and services

  • Education Programs Programs, conferences, workshops and events designed to increase awareness and share knowledge about bleeding disorders with patients, families, and medical professionals in Southern California.
  • Advocacy Services Advocacy on behalf of the bleeding disorders community to amplify their voice on policy, healthcare access, and related matters, delivered in partnership with NBDF and HFA at the national level.
  • Scholarship Program Multi-scholarship program (Christopher Mark Pitkin Memorial, Joshua Kim Advocacy is in Your Blood, Victoria Mendoza Perez Healthcare) awarding funds to members of the bleeding disorders community pursuing education. Over $115,000 awarded during the last decade.
  • Emergency Financial Assistance (EFA) Program Temporary financial relief for families in crisis, covering housing, transportation, food, and utility bills for individuals and families affected by bleeding disorders in Southern California.
  • Medical Alert ID Program Distributes medical alert identification tools to individuals with bleeding disorders to support their safety and emergency care.
  • Family Information Day Annual educational event bringing together families affected by bleeding disorders for information sharing and networking.
  • Family Retreat (Hemochella) Annual family retreat offering opportunities for families facing bleeding disorders to create memories and strengthen community connections. The 2023 'Hemochella' event drew 33 families (114 attendees).
  • Women's Retreat Annual retreat specifically for women affected by bleeding disorders, providing education and community support. The 2024 Women's Retreat drew 90 women.
  • Men's Retreat Event for boys, men, or those who identify as male with a bleeding disorder, or who are male parents, caregivers, spouses, or siblings of someone with a bleeding disorder.
  • Familia de Sangre Conference Annual Spanish-language conference for the bleeding disorders community, described as the country's largest Spanish-speaking conference for bleeding disorders.
  • Bleeding Disorders Conference Annual conference organized by the National Bleeding Disorders Foundation (NBDF) that HFSC participates in and promotes to Southern California community members.
  • Back to School Event Annual event helping families of children with bleeding disorders navigate returning to the classroom, including understanding educational rights (IEP/504 plans) and creating individualized health and academic plans.
  • Community Groups Facilitated community groups connecting individuals and families affected by bleeding disorders in Southern California.
  • Monthly Newsletter Subscription Monthly newsletter delivered online or by mail to subscribers, providing news, events, and updates for the bleeding disorders community.

Quantifiable outcome

  • Over $115,000 in scholarship funds awarded during last decade
  • +1 more outcomes

Companies that use Hemophilia Foundation Southern California

Customer profile

Named customers2 records

Segments4 records

Ideal customer profiles2 records

Hemophilia Foundation Southern California technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Hemophilia Foundation Southern California partnerships and signals

Strategic signal

Partnerships

Eleven partnerships are on record, tiered major, important, core and notable.

  • Hemophilia Federation Alliance (HFA)majorStrategic or Co-development Partner · 6 August 2025HFA is a national organization representing the bleeding disorders community. HFSC partners with HFA on advocacy, education, and policy issues affecting patients including Medicaid/Medicare data privacy concerns.
  • Kendra ScottimportantGTM or Marketing Partner · 3 February 2025Shop for Good partnership where 20% of purchases during designated periods support HFSC programs including Wildfire Relief Fund, Emergency Financial Assistance program, Medical Alert ID program, and educational scholarships.
  • EveryLife Foundation for Rare DiseasesimportantGTM or Marketing Partner · 3 February 2025Partners with HFSC to promote the #RAREis Scholarship Fund providing $5,000 scholarships to 104 rare disease recipients in 2025.
  • National Bleeding Disorders Foundation (NBDF)majorStrategic or Co-development Partner · 5 June 2024NBDF is a national organization working to bleeding disorders community. HFSC works in partnership with NBDF on conferences, advocacy efforts, and policy initiatives at the national level.
  • SanoficoreGTM or Marketing Partner · 9 June 2023Platinum sponsor of HFSC 2023 Family Retreat 'Hemochella'. Sanofi is a pharmaceutical company developing treatments for bleeding disorders.
  • TakedacoreGTM or Marketing Partner · 9 June 2023Platinum sponsor of HFSC 2023 Family Retreat 'Hemochella'. Takeda is a pharmaceutical company developing treatments for bleeding disorders.
  • GenentechimportantGTM or Marketing Partner · 9 June 2023Gold sponsor of HFSC 2023 Family Retreat 'Hemochella'. Genentech develops treatments for rare diseases including bleeding disorders.
  • Hemophilia Federation of America (HFA)coreGTM or Marketing Partner · 9 June 2023Gold sponsor of HFSC 2023 Family Retreat 'Hemochella'. HFA is a national advocacy organization for the bleeding disorders community.
  • OctapharmaimportantGTM or Marketing Partner · 9 June 2023Silver sponsor of HFSC 2023 Family Retreat 'Hemochella'. Octapharma develops and produces human proteins for bleeding disorders treatments.
  • Venice Family ClinicnotableStrategic or Co-development Partner · 28 July 2022Former employer of current Executive Director Rigo Garcia, who served as Director of Health Education providing healthcare access to underserved communities.
  • Hemophilia Treatment Centers Western States RegionalcoreStrategic or Co-development Partner · 8 July 2021HFSC participates in the HTC Western States Regional conference to discuss best practices and care for the bleeding disorders community. Supports HTC sustainability.

Scale indicators5 records

Recent moves6 records

Expansion highlights4 records

Hemophilia Foundation Southern California competitors and assessment

Company assessment

Market position

Competitive moat3 records

Key risks5 records

Key highlights7 records

Customer concentration

Hemophilia Foundation Southern California social profiles

Digital presence

Hemophilia Foundation Southern California financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Hemophilia Foundation Southern California leadership team

Management profile

Number of profiles

Profiles5 records

Hemophilia Foundation Southern California funding detail

Funding detail

Funding overview

Funding rounds

Investors

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Hemophilia Foundation Southern California M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Hemophilia Foundation Southern California

What does Hemophilia Foundation Southern California do?

The Hemophilia Foundation of Southern California is a 501(c)(3) nonprofit patient advocacy foundation that delivers free education, advocacy, support services, scholarships, and emergency financial assistance to individuals and families affected by inherited bleeding disorders (hemophilia A, hemophilia B, von Willebrand disease, inhibitors, rare factor deficiencies, platelet disorders). It runs annual educational conferences and family retreats, funds scholarships, distributes medical alert IDs, and provides emergency relief across nine Southern California counties.

Is Hemophilia Foundation Southern California a public or private company?

Hemophilia Foundation Southern California is a private company. It is classified as nonprofit foundation owned and is currently operating.

When was Hemophilia Foundation Southern California founded?

Hemophilia Foundation Southern California was founded in 1954. It employs 11 to 50 people.

Where is Hemophilia Foundation Southern California based?

Hemophilia Foundation Southern California is headquartered in Pasadena, CA, United States, in the North America region.

How does Hemophilia Foundation Southern California make money?

Three revenue lines are on record. Donations and Fundraising is the primary driver. The others are event-Based Fundraising and emergency Financial Assistance Program.

Does Hemophilia Foundation Southern California have an API?

No public API is recorded for Hemophilia Foundation Southern California.

What industry is Hemophilia Foundation Southern California in?

Hemophilia Foundation Southern California's product category is Patient Advocacy and Community Health Services. Its primary akta.pro industry code is BPAGACAA, Disease-Specific Research & Support (e.g., Cancer, Diabetes, ALS), with a secondary code of EDAAAFAG, Health Promotion & Public Health Education (Community Workshops). Its NAICS code is 813212 and its SIC code is 8090.

Unlock the full company data

50 free credits on sign-up, no credit card required.

Contact sales