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Senate panel considers H293, shifting some health reporting to every three years and clarifying registry data access
Summary
H293 would move some Department of Health reports (including health‑equity reporting) to a three‑year cycle and clarify how cancer and ALS registries may share data with researchers, adding privacy‑board review language alongside institutional review boards.
Committee staff introduced H293 as a Department of Health request bill that would, among other things, change the frequency of certain department reports from annual to every three years and clarify statutory language governing access to disease registries for research.
Legislative counsel said the bill would amend a health‑equity reporting requirement so that the department submits consolidated results to the Legislature every three years beginning in 2028; the…
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