Legal and Regulatory Guidance for Racial/Ethnic Data Disaggregation in Health Data Sets

Legal and Regulatory Guidance for Racial/Ethnic Data Disaggregation in Health Data Sets

Our panel of experts discussed the landscape of rules and regulations that provide guidance – and sometimes confusion – on the collection of racial and ethnic information in a variety of health data sources from national surveys to state health departments to hospital level data.

Presenters included: Ignatius Bau, JD, Health Policy Consultant; Sarah Scholle, Dr.PH, Vice President of Research and Analytics, National Committee for Quality Assurance (NCQA); and Jennifer Park, PhD, Study Director, Committee on National Statistics, National Academies of Sciences, Engineering, and Medicine.

 

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