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Using an Equivalent Protections Framework to Improve Oversight of International Human Subjects Research

Bibliographic Data

ID19516838
AuthorsLiza Dawson (0000-0002-0980-4107, Walter Reed Army Institute of Research, corresponding author), Hunter Jackson Smith (0000-0002-3591-588X, Armed Forces Health Surveillance Center)
Year2026
Volume26
Issue2
Pages99-103
Publication date2026-06-01
Open AccessYes
TypeARTICLE
VenueDeveloping World Bioethics (JOURNAL)
Journal identifiersISSN: 1471-8731 • E-ISSN: 1471-8847
PublisherWiley (PUBLISHER • GB)
DOI10.1111/dewb.70036
PMID42183798
OpenAlexW7162288440
LanguageEN
References cited29

Current US military international research protocols involving human subjects are reviewed, approved, and overseen by both US and regulatory bodies. In some cases host nation research partners are disadvantaged due to slower processing times and redundant protocol reviews when competing for opportunities to conduct clinical trials. This article considers international legal and regulatory tensions between protecting host nations’ patient‐subjects and supporting host nation researchers’ ability to conduct phase 2 and phase 3 clinical trials in support of important military and global health objectives

Disadvantaged · Host (biology) · Human research · Human rights · Human services · Phase (matter) · Protocol (science) · Research ethics · Ethics in Clinical Research · Global Health and Surgery · Torture, Ethics, and Law

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