(a)
In general— The Secretary of Health and Human Services (in this section referred to as the “Secretary”) shall seek to enter into a contract with the National Academies of Sciences, Engineering, and Medicine (referred to in this section as the “National Academies”) not later than 30 days after the date of enactment of this Act, under which the National Academies agree to conduct a study with stakeholders from Federal agencies, State, Tribal, Territorial, and local governments, research institutions, industry, and nonprofit organizations that would review the current system for public health data infrastructure and reporting and provide recommendations on needed data and system improvements for future pandemics and ongoing public health needs.
(b)
Submission of report— The contract under subsection (a) shall require that the study under such subsection be completed, and a report on the resulting recommendations be submitted to the Secretary, the Committee on Health, Education, Labor, and Pensions of the Senate and the Committee on Energy and Commerce of the House of Representatives, not later than 12 months after the date the contract was executed.
(c)
Study topics— The contract under subsection (a) shall require the study under such subsection to—
(1)
review the current public health data systems and the reporting structure for Federal, State, Tribal, Territorial, and local public health information, including vital records;
(2)
review current standards for reporting, quality controls, and transparency of the data;
(3)
examine data gaps and barriers to timely and accurate reporting and identify ways to fill those gaps;
(4)
examine how systems can be accessed and used by a wide range of users, including external researchers;
(5)
examine how different data systems interact and how different data sources can be integrated;
(6)
examine nontraditional data sources or alternative data gathering methods that could be used to complement traditionally collected data;
(7)
identify needed improvements to the public health data systems and structure, especially with regard to the needs of Tribal systems;
(8)
identify core elements of a “minimum data set” that might be used for State population surveillance, including demographic components that are necessary to ensure health equity in public health decision making;
(9)
examine how surveillance systems can be explicitly designed to ensure underserved populations (which may include racial and ethnic minorities, immigrants, individuals in nursing homes, other institutionalized populations, and individuals experiencing homelessness) are included in reporting;
(10)
consider how traditional and nontraditional data might be used to promote health equity across the United States and reduce racial, Tribal, and other demographic disparities;
(11)
examine data gaps and barriers to collecting, analyzing, and using demographic data to characterize the COVID–19 pandemic for public health action and research to improve public health actions and identify ways to fill those gaps; and
(12)
report on what is known based on existing data about how COVID–19 is impacting subgroups of the population with respect to access to testing, treatment, and vaccination (hospitalization and access to drugs and medical equipment), and health outcomes (morbidity and mortality).
(d)
Disaggregation of data— To the extent feasible, the contract under subsection (a) shall require data to be disaggregated by race, ethnicity, age, gender, disability, geography, language, socioeconomic status, and other factors.
(e)
Authorization of appropriations— To carry out this section, there is authorized to be appropriated $1,000,000, to remain available until expended.