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VT H0293
Bill
Status
4/15/2025
Primary Sponsor
Eric Maguire
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AI Summary
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Department of Health health equity data reports to the legislature reduced from annually to every three years, beginning in 2028, with reports due by January 15
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Cancer registry confidentiality provisions updated to require approval from an institutional review board or privacy board (under 45 C.F.R. § 164.512) instead of an academic committee for human subjects protection when sharing data with researchers
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Amyotrophic lateral sclerosis (ALS) registry disclosure requirements similarly updated to require institutional review board or privacy board approval for researcher data sharing agreements
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Commissioner must obtain written assurances (rather than a written agreement) from registries, agencies, or researchers that identifying information will remain confidential before releasing cancer registry data
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Effective date: July 1, 2025
Legislative Description
An act relating to health equity data reporting and registry disclosure requirements
Last Action
Referred to Committee on Health and Welfare per Temporary Senate Rule 44A
1/6/2026