Though the National Aeronautics and Space Administration’s collection of disaggregated genetic data for occupational surveillance and research raises numerous privacy concerns, the Genetic Information Nondiscrimination Act of 2008 allows genetic information to be used to develop personal pharmaceuticals.

Questions about data privacy need to be addressed when research institutions negotiate with companies developing mobile health applications. Commercial terms of use and data sharing notifications should be reviewed before use in human subject research settings.

Social and behavioral data contained in electronic health records are essential for studying health disparities. Can researchers avoid bias when collecting, analyzing, and using such data?

This letter responds to readers’ recent letter to the editor.

Telesurgery is a form of global health diplomacy, and negotiations between LMICs and HICs can have transnational consequences.

Dania Pagarkar joins Ethics Talk to discuss her article, coauthored with Drs Erin Harrop and Lisa Erlanger: “How Should We Approach Body Size Diversity in Clinical Trials?”

Telehealth offers access and quality opportunities for some patients with mental illness.

Dr Andrew P. Smith joins Ethics Talk to discuss his article, coauthored with Dr Hasah Alheneidi: “The Internet and Loneliness.”

Consumption and trade of wild animals present major zoonotic disease transmission risks.

Organizations’ architecture and communities’ waste stream designs situate how well industrial hygiene practices support or undermine individuals’ and communities’ pathogenic vulnerability.