Medical Device Nonvisual Accessibility Act of 2025 establishes nonvisual accessibility standards for certain medical devices.
The Medical Device Nonvisual Accessibility Act of 2025 amends the Federal Food, Drug, and Cosmetic Act to establish nonvisual accessibility standards for certain medical devices with digital interfaces. The act requires these devices to be as effective for blind or low-vision individuals as they are for those without visual impairments. The Secretary of Health and Human Services must issue regulations to implement these standards and provide training to manufacturers.
Included in complete analysis
- Overview
- Core Provisions
- Implementation
- Impact
- Legal Framework
- Critical Issues
See what it does, who it affects, and the critical issues in plain language. Free, 30 seconds.