Failure Analysis Testing: Methods, Standards, and Root Cause Investigation
How labs trace a cracked, leaking, or worn part back to its root cause, and which standards shape the work
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How labs trace a cracked, leaking, or worn part back to its root cause, and which standards shape the work
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Here's how third-party labs verify supplement safety, potency, and label accuracy under US regulations
Explore how Maintenance, Repair, and Operations (MRO) supports compliance, safety, and reliability, and how labs enable testing and calibration
An in-depth analysis of the FDA's 2015 guidance for reprocessing reusable medical devices, driven by patient safety concerns in health care
Achieving a high Sterility Assurance Level (SAL) is crucial for ensuring the safety of medical devices, pharmaceuticals, and other sterile products.
A comprehensive overview of irritation testing for medical devices, from its scientific basis and a tiered testing approach to the regulatory landscape
A detailed analysis of food recalls, from the microbiological and chemical origins to the regulatory landscape, providing essential insights for lab professionals
A comprehensive guide to the critical safety standards and FDA regulations governing both edible and inedible dessert decorations for professionals
Discover how metallurgical testing supports failure analysis, quality assurance, and material verification in laboratory environments
Practical guidance for ISO/IEC 17025–accredited labs supporting manufacturers, retailers, and brand owners in meeting safety, quality, and compliance requirements
“Labs succeed when they build a collaborative and accountable culture,” says Cheryl Bowden on fostering strong client relationships in the environmental testing industry
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