Rhode Island General Laws Title 23. Health and Safety § 23-87.1-2. Establishment

(1) Convene public hearings, make inquiries, and solicit comments from the general public in Rhode Island to assist the council with a first-year landscape or survey of the needs of rare disease patients, caregivers, and providers in the state.

(2) Provide testimony and comments on pending legislation and regulations before the legislature and other state agencies that impact Rhode Island's rare disease community.

(3) Consult with experts on rare diseases to develop policy recommendations to improve patient access to, and quality of, rare disease specialists, affordable and comprehensive healthcare coverage, relevant diagnostics, timely treatment, and other needed services.

(4) Research and make recommendations to state agencies and insurers that provide services to persons with a rare disease on the impact of prior authorization, cost-sharing, tiering, or other utilization management procedures on the provision of treatment and care for patients.

(5) Establish best practices and protocols to include in-state planning related to natural disasters, public health emergencies, or other emergency declarations to enable continuity of care for rare disease patients and ensure safeguards against discrimination for rare disease patients are in place.

(6) Evaluate and make recommendations to implement improvements to newborn infant screening programs.

(7) Evaluate and make recommendations to improve Medicaid coverage of drugs for rare disease patients, including engagement with the drug utilization review board, to improve coverage of diagnostics, and facilitate access to necessary healthcare providers with expertise in the treatment of rare diseases.

(8) Publish a list of existing, publicly accessible resources on research, diagnosis, treatment, and education relating to the rare diseases on the council's website.  For purposes of this chapter, “rare disease” or “orphan disease” means a disease that affects fewer than two hundred thousand (200,000) people in the United States.

(9) Identify areas of unmet need for research and opportunities for collaboration across stakeholders that can inform future studies and reports by the council.

(10) Identify and distribute educational resources for healthcare providers to foster recognition and optimize treatment of rare diseases.

(11) Research and identify best practices to reduce health disparities and achieve health equity in the research, diagnosis, and treatment of rare diseases.

(12) Research and identify best practices to ensure continuity of care for rare disease patients transitioning from child/youth services to adult care.