Abstract
After reading the educational posters and completing the quiz, participants will be able to: Understand the role of cancer registry software in supporting research and data collection: Learning from our Children: Adapting Data Management in an Adult World. Building a Melanoma Research Registry Within a Cancer Reporting Software. Describe how data can be used to identify the need for cancer genetic services and interventions in target populations: Mapping Cancer Incidence among Hereditary Cancer Types in Michigan, 2014–2018. Understand the importance of studies and evaluations for quality control at the local and national levels. Casefinding: Beyond Path Reports. Results of Year 2 Data Quality Evaluation of CDC's National Program of Cancer Registries: Weighing the Evidence, Identifying Research Gaps, and Evaluating Outputs of a Prevention Research Agenda.