The California Health Care Foundation is an independent, nonprofit philanthropy that works to improve the health care system so that all Californians have the care they need.
CHCF publishes reports, articles, issue briefs, explainers, data snapshots, infographics, fact sheets, and other resources to help make meaningful change in California’s health care system.
The California Health Care Foundation is an independent, nonprofit philanthropy that works to improve the health care system so that all Californians have the care they need.
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Participating clinicians learn about leadership and management skills necessary to help them improve the operations of California’s safety-net institutions and the state’s overall health care system.
The California Health & Human Services Agency has announced the designation of nine entities as Qualified Health Information Organizations to support the state’s health data exchange framework.
California has a lot of work to do to build a representative physician workforce. Latinos account for just 6% of physicians, despite making up 39% of the state’s population.
This fact sheet provides general information and resources for operators interested in learning more about CalAIM and how its Community Supports program may support the populations they serve.
Pivoting from Whole Person Care to CalAIM has been a challenge for county health administrators. In this brief, we talked to people on the ground who describe what has worked and what still needs improvement in the implementation of CalAIM.
This resource from Transforming Care Partners describes the key drivers of California’s progress in palliative care and remaining opportunities to build on and accelerate this growth to meet future needs.
This resource from Transforming Care Partners describes the key drivers of California’s progress in palliative care and remaining opportunities to build on and accelerate this growth to meet future needs.
This resource from Transforming Care Partners describes the key drivers of California’s progress in palliative care and remaining opportunities to build on and accelerate this growth to meet future needs.
This paper examines the policy, legal, and technical components that must be addressed to grow consent management services from promising county-level pilots to a statewide information exchange.