Regulates AI devices in eye assessments, requiring synchronous/asynchronous provider-patient interaction, medical history collection, and disclosure about assessment limits. Requires providers to verify patient details, maintain records, adhere to care standards, and not rely solely on assessment data. Authorizes penalties for violations.
Good coverage — Comprehensive governance measures or mitigations with clear procedures relating to the risk subdomain are explicitly described.
Minimal coverage — Brief mention but no specific mitigations, recommendations or governance measures relating to the risk subdomain are described.
All other risk subdomains had no coverage in this document.
Risk Coverage Summary
The document has minimal coverage of AI risk domains, with limited focus on system safety and failures (7.3 - lack of robustness) and human-computer interaction (5.1 - overreliance). The legislation primarily addresses procedural safeguards for AI-assisted eye assessments rather than comprehensive AI risk mitigation. Coverage is concentrated in ensuring clinical standards and preventing inappropriate reliance on automated assessments.
Good coverage — Comprehensive governance measures or mitigations with clear procedures relating to the sector are explicitly described.
All other sectors had no coverage in this document.
Sectors Summary
This legislation specifically governs AI use in the Health Care and Social Assistance sector, with focused regulation of eye care services including optometry and ophthalmology. The document establishes comprehensive requirements for providers using AI-based assessment mechanisms to conduct eye assessments and generate prescriptions.
Hard Law
Legislative Status Summary
This is a binding state statute enacted by the Rhode Island legislature with mandatory requirements, civil penalties up to $10,000 per violation, and enforcement mechanisms through the Department of Health and Attorney General's office.
Proposer
Target
Enforcer
Monitor
Lifecycle stages covered by the documents, as defined in the OECD Framework for the Classification of AI Systems
AI Lifecycle Summary
The document primarily focuses on the Deploy and Operate and Monitor stages of the AI lifecycle. It establishes requirements for how AI-based assessment mechanisms must be deployed in clinical practice and mandates ongoing operational standards including record-keeping, patient verification, and adherence to clinical care standards during use.
Terms relating to technical scope that are mentioned or implicitly referenced in the document
Technical Scope Summary
The document explicitly mentions AI devices as a type of assessment mechanism but does not define or distinguish between AI models, AI systems, or specific categories like frontier AI, general purpose AI, or foundation models. It takes a broad, technology-neutral approach to regulating automated assessment mechanisms regardless of their underlying AI architecture.
Document data from AGORA, CSET Emerging Technology Observatory.