When “Healthy” Turns Hazardous: What a Drug-Resistant Salmonella Outbreak in Supplements Means for Manufacturers
Dietary supplements are marketed as tools for wellness — capsules to boost immunity, powders to enhance nutrition, herbal extracts to
A Lighter Touch, Heavier Responsibility: What FDA’s Wellness-Device Shift Really Means for Manufacturers
For years, the “wellness device” space has lived in a strange middle ground. On one side: booming consumer demand for
From Code to Confidence: What FDA’s Shifting Digital Health Framework Means for Device Developers
Digital health has officially moved from the edges of medical device innovation to its center. Software now guides clinical decisions.
A Lighter Touch, Heavier Responsibility: What FDA’s Easing of Wellness Device Regulations Really Means for Manufacturers
In recent years, the line between “medical device” and “wellness technology” has grown increasingly blurred. Fitness trackers measure heart rhythm.
When Water Safety Becomes Local Leadership: How States Are Stepping Up to Protect Fresh Water — and What It Means for Testing, Utilities, and Public Trust
For decades, water quality management in the United States operated under a largely federal framework: the U.S. Environmental Protection Agency
When Microns Matter: Why Micro-Scale Leak Testing Is Becoming a Critical Pillar of Medical Device Safety
In medical device manufacturing, failure rarely announces itself loudly. It doesn’t always appear as a broken component, a visible defect,
