S. 792 would amend the Public Health Service Act to improve the National Program of Cancer Registries by expanding data collection and allowing data sharing for public health objectives, while preserving the confidentiality of patients.
Detailed Summary
Improvement of the National Program of Cancer Registries Act - Amends the Public Health Service Act to revise requirements for statewide cancer registries and require the inclusion in such registries of information on: (1) the highest level of education attained by adults with cancer; (2) sources of payment by individuals for the costs of cancer diagnosis and treatment; and (3) the history of alcohol and tobacco use by individuals with cancer.
Requires the Director of the Centers for Disease Control and Prevention (CDC), to: (1) develop standards for collection of data elements for state cancer registries; (2) develop inter-operability and security standards for data exchange and integration between state cancer registries and any cancer registry and another federal registry for non-cancer diseases; and (3) provide a basic electronic collection tool to facilitate standardized data collection.
Requires the Secretary of Health and Human Services to facilitate coordination of the National Program of Cancer Registries with other federally-supported registry programs, including infectious disease registries, environmental disease registries, and other non-cancer, chronic disease registries.
Status of the Legislation
Latest Major Action: 4/2/2009: Referred to Senate committee. Status: Read twice and referred to the Committee on Health, Education, Labor, and Pensions.
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