Bill > H1443

This bill establishes a statewide Parkinson's disease registry and mandates reporting requirements for healthcare professionals. Beginning January 1, 2027, physicians and advanced practice registered nurses (APRNs) who diagnose or treat patients for Parkinson's disease or atypical parkinsonism must report specific information, including nationally recognized performance measures, to this registry. The bill also provides limited liability protection for these professionals against any claims arising from their reporting to the registry. Furthermore, it modifies the Parkinson's Disease Research Board by requiring the President of the Senate and the Speaker of the House of Representatives to each appoint one member, revises membership qualifications and terms, and expands the annual report to include data on the incidence and prevalence of Parkinson's disease by county, registry statistics, and demographic information. The University of South Florida's Institute for Parkinson's Disease, subject to funding, will be responsible for establishing and maintaining the statewide registry and a dedicated public website by January 1, 2028, which will feature downloadable annual reports and other relevant information.

Budget and Finance, Health and Social Services

Health & Human Services Committee (House), Health Care Budget Subcommittee (House), Health Professions & Programs Subcommittee (House)

https://www.flsenate.gov/Session/Bill/2026/1443