From official state and federal legislative records. Informational only, not legal advice.
Signed — now law
The governor signed it. This is now an official law.
The governor signed it. Nothing left to watch.
In plain words
AI summaryWritten by AI from the bill text. Check the official text before relying on it.
An act to establish the rare disease task force within the mississippi rare disease advisory council; To provide that the purpose of the task force is to identify gaps in care, evaluate funding and insurance coverage practices, advise policymakers on evidence-based solutions, and ensure fair, timely, and equitable access to rare disease therapies in this state; To provide for the membership, powers and duties of the task force; To require the task force to make an annual report to certain public officials; To amend section 1 of house bill no. 1622, 2026 regular session, to replace certain instances of the term "license" with "exemption" for the sake of administrative efficiency; And for related purposes.