The Cancer Registries Program supports countries in establishing and bolstering population-based cancer registries to track cancer data, focusing on a combination of strengthening existing registries, building new ones where appropriate, and offering technical assistance and training activities. Our goal is to support a sustainable registry system that informs data-driven planning, including informing cancer control and prevention activities, prioritization and budgeting, and policy development
This Gender Equity Resource Collection provides information on incorporating a gender lens into health data collection, analysis, and use. Here you can find training materials, publications, and technical tools covering topics such as gender concepts and definitions, gender-equitable data collection...
