What are the two main funding sources for population-based Cancer Care Registries in the US?

The two main funding sources for population-based Cancer Care Registries in the United States are the National Cancer Institute (NCI) and the Centers for Disease Control and Prevention (CDC).

The NCI plays a crucial role in cancer research and provides significant funding and resources for various cancer-related initiatives, including population-based registries that collect data on cancer incidence, treatment, and outcomes. This funding supports research that aims to understand cancer trends and improve public health responses to cancer care.

The CDC, on the other hand, contributes to cancer control initiatives that are instrumental in funding cancer registries. Through its partnerships and programs, the CDC helps implement surveillance strategies that ensure comprehensive cancer data collection, which is essential for public health planning and policy-making.

Together, these two organizations facilitate the infrastructure needed for effective cancer data collection, management, and dissemination, which is vital for understanding cancer patterns and guiding interventions at both the state and national levels.