MedTech AI Regulation in the U.S., EU, and UK: How Testing Labs Must Evolve to Support AI-Enabled Medical Devices
Artificial Intelligence (AI) has moved from being a futuristic concept to a practical backbone of modern medical technology. From diagnostic
Shutdown Signals: How the U.S. Government Shutdown Impacts FDA Oversight — and Why Independent Testing Matters More Than Ever
In times of political gridlock, few ripple effects are as consequential as those caused by a federal government shutdown. While
EPA’s Proposed Stricter PFAS Standards: What It Means for Water Utilities — and How CMDC Labs Can Help
For decades, per- and polyfluoroalkyl substances (PFAS) — often called “forever chemicals” — have been quietly accumulating in water systems
Bright Colors, Hidden Risks: What Food Dyes Reveal About Modern Ingredients — And How Testing Keeps Them Safe
Bright reds, electric blues, and vivid yellows are the hallmark of modern foods — from candies and cereals to energy
When Trade Policy Disrupts the Supply Chain: How Medical Device Testing Adapts Under Tariff Pressure
The medical device industry thrives on global collaboration. Components may be designed in Germany, molded in Malaysia, sterilized in the
Food Allergies and Labeling: Why Allergen Verification Is the Cornerstone of Consumer Trust
For millions of Americans, reading a food label is more than a routine—it’s a matter of safety. The U.S. Food
