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VT H0293

Bill

Status

Engrossed

4/15/2025

Primary Sponsor

Eric Maguire

Click for details

Origin

House of Representatives

2025-2026 Session

AI Summary

  • 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

  • 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

  • Amyotrophic lateral sclerosis (ALS) registry disclosure requirements similarly updated to require institutional review board or privacy board approval for researcher data sharing agreements

  • 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

  • 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

Committee Referrals

Health and Welfare1/6/2026
Rules4/17/2025
Human Services2/20/2025

Full Bill Text

No bill text available