Sterile Supply vs. Emissions: How Labs Must Adapt to EtO Relief
On July 17, 2025, the White House issued a proclamation that affects the entire medical device sterilization industry. It gave
Tariff Pressure: What U.S. Manufacturers Must Prepare For
Understanding the Impact of U.S. Tariffs on Chinese Medical Devices — and How Labs Like CMDC Can Help Introduction: The
The Hidden Color Code: Why Synthetic Dye Testing Is a Public Health Imperative
Introduction: What’s Behind the Colors? One in five food and beverage products in the U.S. contains synthetic dyes — yet
Food Safety Gets Real in Florida: The New Role of Environmental Testing
Florida’s Department of Health is intensifying its food safety oversight. With new regulations placing stricter requirements on surface testing, microbial
Why FDA Labeling Standards for AI Medical Devices Can’t Wait
Artificial intelligence (AI) is no longer a futuristic concept in medicine — it’s embedded in today’s diagnostics, imaging, surgical assistance,
What 98 Contaminated Sites Mean for Water Testing Protocols
PFAS Found at 98 U.S. Locations – Implications for Environmental Testing Labs In July 2025, new data from ongoing AFFF
