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Engaging Vulnerable Populations in Research: Building Ethical, Inclusive, and Trustworthy Clinical Studies
Introduction: Inclusion Begins with Ethical Engagement In clinical research, the term “vulnerable populations” describes individuals who may be at risk of coercion, manipulation, or harm due to limited autonomy, health literacy, socioeconomic disadvantage, or institutional dependence. Examples include individuals with cognitive limitations, students or employees under authority, people with limited language proficiency, or those experiencing social or economic marginalizat
6 days ago3 min read


The Advantages of Using U.S.-Based CROs for Study Data Collection
For medical device and wearable technology developers, the success of a clinical research study often hinges on one factor: the quality...
Oct 93 min read
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