Texas HB1884 establishes a sickle cell disease registry to collect and maintain records of cases for treatment and research.
Texas HB1884 creates a sickle cell disease registry to serve as a central repository of case data. The registry will include records of all cases in the state and other relevant information. Health care facilities must provide necessary data to the department, which may use it to compile studies and reports. The department will also submit annual reports to the legislature. The executive commissioner will develop guidelines to ensure data collection and confidentiality align with relevant laws and regulations.
Included in complete analysis
- Overview
- Core Provisions
- Implementation
- Impact
- Legal Framework
- Critical Issues
See what it does, who it affects, and the critical issues in plain language. Free, 30 seconds.