The bill, titled "Rita Littlefield Chronic Kidney Disease Centralized Resource Center," establishes a new resource center within the Health and Human Services Commission aimed at providing comprehensive information and resources related to chronic kidney disease (CKD) and related illnesses. The center will serve as a centralized system where individuals can obtain information on CKD, its clinical stages, and opportunities for clinical trials. It will also maintain a kidney health clinical trials registry to help patients and their families access educational information about clinical trials based on the patient's specific condition.

Additionally, the bill outlines the administration and operation of the resource center, emphasizing the need for a comprehensive approach to provide accessible information on CKD awareness, prevention, and treatment options. The commission is tasked with ensuring that the information is available in both English and Spanish and is required to collaborate with the Chronic Kidney Disease Task Force to maintain relevant resources on its website. The commission may also solicit gifts, grants, and donations to support the implementation of the center. The bill is set to take effect on September 1, 2025, contingent upon legislative appropriations.

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