Resource Library

The purpose of this guide is to provide in-depth information to facilitate implementation of the Race, Ethnicity, Language, and Disability (REALD) demographic data collection standards. This guide also includes information to support analysis and reporting of REALD data.

The Office of Management and Budget published a proposed rule on August 18 with potentially substantial positive ramifications for the Federal statistical system. Orvis and Leslie will overview and respond to questions on the regulation, which is key milestone in implementing Title III of the Foundations for Evidence-Based Policymaking Act of 2018 (Evidence Act). 

Describes literature review of health plan collection of race and ethnicity data and stakeholder suggestions for improving collection.

Discusses barriers in accessing disaggregated racial/ethnic data in federal data sets and identifies opportunities to expand availability of data

Presents the recommendations and calls to action to advance data systems across public and private sectors to improve health equity.

Summary of recommendations from the full report Charting a Course for an Equity-Centered Data System.

This report reviews findings from a national study on data collection, processing and dissemination practices for population health surveys, identifying barriers to disaggregating certain groups and providing recommendations to improve the availability of subgroup data.

Describes NIST framework to better manage risks to individuals, organizations, and society associated with artificial intelligence (AI).

Describes proposals in the "Health Data, Technology, and Interoperability: Certification Program Updates, Algorithm Transparency, and Information Sharing“ proposed rule.

Describes flexibilities of and best practices for collection of race and ethnicity data in compliance with OMB 15.