Navigating Diversity: Optimizing Data Collection for Cardiovascular Health

Author:

Shah Kevin S.ORCID,Makaryus Amgad N.ORCID

Publisher

Elsevier BV

Reference22 articles.

1. U.S. Food and Drug Administration (FDA). Collection of race and ethnicity data in clinical trials: guidance for industry and Food and Drug Administration Staff. Available at: https://www.fda.gov/regulatory-information/search-fda-guidance-documents/collection-race-and-ethnicity-data-clinical-trials. October 2016. Accessed August 11, 2024.

2. Office of Management and Budget. Revisions to the standards for the classification of federal data on race and ethnicity. October 30, 1997. Available at:https://obamawhitehouse.archives.gov/omb/fedreg_1997standards. Accessed August 11, 2024.

3. Office of the Assistant Secretary for Planning and Evaluation (ASPE), U.S. Department of Health and Human Services (HHA). HHS implementation guidance on data collection standards for race, ethnicity, sex, primary language, and disability status. Available at:https://aspe.hhs.gov/reports/hhs-implementation-guidance-data-collection-standards-race-ethnicity-sex-primary-language-disability-0. Accessed August 11, 2024.

4. Guidance for industry on the collection of race and ethnicity in clinical trials; availability;Fed Regist,2005

5. National Institutes of Health (NIH). Racial and ethnic categories and definitions for NIH diversity programs and for other reporting purposes. Available at: https://grants.nih.gov/grants/guide/notice-files/not-od-15-089.html. Accessed August 11, 2024.

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