Parkinson’s Disease Registry
What changed between versions
Reporting requirements were expanded to include osteopathic physicians and advanced practice registered nurses in addition to physicians.
New statutes were created to specifically mandate reporting and provide liability protection for osteopathic physicians and advanced practice registered nurses.
A new requirement was added for the institute to create and maintain a public website dedicated solely to the registry, starting in 2028.
The entity responsible for the registry changed from an external 'Consortium for Parkinson's Disease Research' to the 'Institute for Parkinson's Disease at the University of South Florida'.
The composition of the Parkinson's Disease Research Board was revised to include members appointed by the Senate and House, as well as representatives from participating universities and academic medical centers.
The reporting start date remains January 1, 2027, but the public website launch was set for January 1, 2028, and the first annual report on the website for January 1, 2029.