Would you question health decisions made by a 37-year old Black woman whose great-grandfather died in the US Public Health Service Syphilis Study at Tuskegee?

Recent popular interest in Henrietta Lacks has prompted interest in better engaging AA nurses and communities.

This article addresses intergenerational trauma transmission, focusing on Japanese American and Southeast Asian American communities.

Financial relationships are common, and ethical questions rightly emerge about how conflicts of interest compromise investigators’ approaches to research.

“Race” is a product of European-American views of phenotypic and cultural differences and continues to influence Native health decision making.

The University of Global Health Equity aims to provide the tools and technology to develop the skills students need to improve fragile health systems.

Although the World Health Organization defines infertility as a disease, insurance coverage gaps generate disparities in access to care and treatment, especially for tubal factor infertility and oncofertility.

Global health outreach programs can risk benefitting students from resource-rich areas of the world more than the patients in resource-poor areas of the world. This month’s episode of Ethics Talk explores an alternative to academic health center-based health outreach programs.

Clinician-researchers deeply invested in data gathering are still obliged to respect a patient-subject’s right to stop being in research.

Guidelines are needed to help ensure that trainee, institutional, and faculty engagement in global health is ethically appropriate and mutually beneficial for all involved.