FDA’s Nonclinical Testing Rule: What It Means for CROs Offering NAMs
US FDA's direct final rule rewrites drug and biologics regulations to cover in vitro, in silico, and organ-chip studies, giving NAM-ready CROs a clearer opening with sponsors
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US FDA's direct final rule rewrites drug and biologics regulations to cover in vitro, in silico, and organ-chip studies, giving NAM-ready CROs a clearer opening with sponsors
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Learn about the essential chemistry and microbiology tests required to bring complex plant-based meat and dairy formulations safely to market
Premium juices are prime targets for economic fraud. Here's how ISO 17025 labs catch fake sugars and dilution before products hit the shelf
Per Kari Barnes, "the strongest programs treat sustainability, food-contact safety and package performance as parallel design requirements"
Learn how independent laboratory validation proves your processing equipment is safe, cleanable, and ready for the official 3-A Symbol
With the 2026 Cyclospora outbreak linked to fresh lettuce, learn why this parasite evades traditional swabs and how FDA molecular testing can secure your produce supply chain
Explore modern pathogen detection technologies, FDA traceability mandates, and the shift to rapid food safety
Ensuring that food contact substances do not leach harmful chemicals into food is essential for protecting public health
Non-compliant retail packaging is a hidden drain on thin e-commerce margins. Third-party laboratory validation helps vendors eliminate penalties and secure certified status
Partner with this California-based FDA-registered contract lab for deformulation and advanced GC-MS/NMR chemical analyses
With strict EU PPWR and EmpCo deadlines, manufacturers must anchor environmental claims in standardized LCA frameworks to protect market access
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