Accelerating INDs Without Animals: How CROs Can Capitalize on FDA’s New Methodologies
A landmark FDA direct final rule officially clears the path for organs-on-chips and in vitro models. Advanced CROs can capture the shifting outsourcing market
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A landmark FDA direct final rule officially clears the path for organs-on-chips and in vitro models. Advanced CROs can capture the shifting outsourcing market
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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
When standard methods fall short, discover how contract labs excel in custom test program development for novel glass and ceramic materials
OECD 301 testing determines the biodegradability of chemical substances, supporting regulatory compliance, environmental responsibility, and product innovation across global markets
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