Establishes the Mississippi Parkinson's Disease Research Registry within the State Department of Health.
The bill establishes the Mississippi Parkinson's Disease Research Registry within the State Department of Health, under the direction of the State Health Officer. It mandates the collection of data on the incidence and prevalence of Parkinson's disease and Parkinsonisms in Mississippi, including patient demographics, geography, diagnosis, and deduplication information. Patients can opt out of data collection after reviewing relevant documents. The registry data is confidential and cannot be used in legal proceedings.
Included in complete analysis
- Overview
- Core Provisions
- Implementation
- Impact
- Legal Framework
- Critical Issues
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