THE BILL ITSELF
CS/SB 1684
Parkinson’s Disease Registry
Florida Senate - 2026 CS for SB 1684 By the Appropriations Committee on Health and Human Services; and Senator Calatayud 603-02961-26 20261684c1
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A bill to be entitled
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An act relating to the Parkinson’s disease registry;
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creating ss. 458.352, 459.075, and 464.0124, F.S.;
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requiring physicians, osteopathic physicians, and
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advanced practice registered nurses, respectively, to
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report certain information to the Parkinson’s disease
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registry; providing limited liability for physicians
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and advanced practice registered nurses under certain
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circumstances; amending s. 1004.4352, F.S.; revising
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the membership of the Parkinson’s Disease Research
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Board; requiring that annual reports of the board
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include specified information beginning on a specified
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date; requiring the Institute for Parkinson’s Disease
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at the University of South Florida, subject to
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appropriation, to establish and maintain a statewide
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Parkinson’s disease registry for specified purposes;
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providing requirements for the registry; requiring
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certain physicians and advanced practice registered
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nurses to report specified information to the registry
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regularly; requiring the institute, beginning on a
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specified date, to create and maintain a public
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website dedicated solely to the registry; specifying
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requirements for the website; requiring that the
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website be updated by a specified date and annually
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thereafter; providing an effective date.
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Be It Enacted by the Legislature of the State of Florida:
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Section 1. Section 458.352, Florida Statutes, is created to
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read:
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458.352 Parkinson’s disease registry; reporting
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requirement.—
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(1) Beginning January 1, 2027, each physician who diagnoses
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or treats a patient for Parkinson’s disease shall report to the
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statewide Parkinson’s disease registry, established pursuant to
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s. 1004.4352, information containing nationally recognized
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Parkinson’s disease performance measures.
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(2) A liability of any kind or character for damages or
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other relief may not arise or be enforced against a physician by
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reason of having provided such information to the statewide
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Parkinson’s disease registry.
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Section 2. Section 459.075, Florida Statutes, is created to
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read:
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459.075 Parkinson’s disease registry; reporting
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requirement.—
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(1) Beginning January 1, 2027, each physician who diagnoses
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or treats a patient for Parkinson’s disease shall report to the
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statewide Parkinson’s disease registry, established pursuant to
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s. 1004.4352, information containing nationally recognized
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Parkinson’s disease performance measures.
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(2) A liability of any kind or character for damages or
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other relief may not arise or be enforced against a physician by
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reason of having provided such information to the statewide
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Parkinson’s disease registry.
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Section 3. Section 464.0124, Florida Statutes, is created
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to read:
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464.0124 Parkinson’s disease registry; advanced practice
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registered nurse reporting requirement.—
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(1) Beginning January 1, 2027, each advanced practice
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registered nurse who diagnoses or treats a patient for
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Parkinson’s disease shall report to the statewide Parkinson’s
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disease registry, established pursuant to s. 1004.4352,
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information containing nationally recognized Parkinson’s disease
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performance measures.
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(2) A liability of any kind or character for damages or
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other relief may not arise or be enforced against an advanced
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practice registered nurse by reason of having provided such
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information to the statewide Parkinson’s disease registry.
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Section 4. Paragraphs (b) and (e) of subsection (4) of
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section 1004.4352, Florida Statutes, are amended, and subsection
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(5) is added to that section, to read:
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1004.4352 Parkinson’s disease research.—
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(4) CONSORTIUM FOR PARKINSON’S DISEASE RESEARCH.—
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(b) The Parkinson’s Disease Research Board is established
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to direct the operations of the consortium. The board shall be
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composed of one member appointed by the President of the Senate,
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one member appointed by the Speaker of the House of
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Representatives, and members representing each participating
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university or academic medical center, appointed by the
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president or chief executive officer of each participating
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university or academic medical center. Board members , other than
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those appointed by the President of the Senate or the Speaker of
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the House of Representatives, must have experience as a movement
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disorder specialist and in informatics or population health
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research and Parkinson’s disease research in a variety of
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scientific fields, including, but not limited to, neurology,
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psychology, nutrition, and genetics . Members shall be appointed
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to 3-year 4-year terms and may be reappointed to serve
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additional terms. The chair shall be elected by the board from
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among its members to serve a 2-year term. The board shall meet
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at least semiannually at the call of the chair or, in his or her
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absence or incapacity, the vice chair. Four members constitute a
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quorum. A majority vote of the members present is required for
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all actions of the board. The board may prescribe, amend, and
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repeal a charter governing the manner in which it conducts its
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business. Board members shall serve without compensation, but
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are entitled to receive reimbursement for travel expenses by the
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consortium or the organization he or she represents in
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accordance with s. 112.061.
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(e) By October 15 of each year, the board shall issue a
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report to the Governor, the President of the Senate, and the
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Speaker of the House of Representatives on research projects,
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research findings, and community outreach initiatives conducted
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or funded by , and future plans for the consortium. Beginning on
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October 15, 2028, and annually thereafter, the report must
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include a summary update on the incidence and prevalence of
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Parkinson’s disease in this state by county, how many records
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have been included and reported to the registry, and demographic
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information, such as patients by age, gender, and race.
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(5) PARKINSON’S DISEASE REGISTRY.—
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(a) Subject to a specific appropriation, the Florida
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Institute for Parkinson’s Disease at the University of South
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Florida shall establish and maintain a statewide Parkinson’s
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disease registry to ensure that the Parkinson’s disease
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performance measures required to be submitted under paragraph
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(b) are maintained and available for use to improve or modify
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the Parkinson’s disease care system, ensure compliance with
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standards and nationally recognized guidelines, and monitor
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Parkinson’s disease patient outcomes.
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(b) Physicians licensed under chapter 458 or chapter 459,
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pursuant to ss. 458.352 and 459.075, and advanced practice
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registered nurses licensed under chapter 464, pursuant to s.
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464.0124, shall regularly report to the statewide Parkinson’s
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disease registry information containing nationally recognized
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Parkinson’s disease performance measures.
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(c) Beginning January 1, 2028, the Institute for
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Parkinson’s Disease at the University of South Florida shall
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create and maintain a public website dedicated solely to the
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Parkinson’s disease registry which must include, at a minimum,
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downloadable annual reports on the incidence and prevalence of
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Parkinson’s disease, information on the consortium, and other
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information as determined by the board. The website must be
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updated by January 1, 2029, and annually thereafter.
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Section 5. This act shall take effect July 1, 2026.