Improving DATA in Public Health Act

This bill requires healthcare providers, labs, and public health agencies to report standardized electronic health data to the CDC, including real-time information on cases, lab results, and demographic details like race, disability status, and housing. It mandates that data collection and sharing follow specific technical standards to improve quality, address health disparities, and ensure demographic data is captured accurately. The bill establishes an advisory committee to guide implementation and allocates $10 million annually (2024-2026) to fund best practices for improving data collection methods, particularly for underserved communities. It also includes safeguards to protect patient privacy and prevent unnecessary duplication of reporting burdens.