The new cleanroom at our global headquarters in Salt Lake City, Utah, was designed for today's rigorous contamination control expectations, driven by EU GMP Annex 1. Learn More
Blog Post 12 – Bridging Analytical Gaps: Identification of GC/MS Impurities from External Labs 3 min reading time At Nelson Labs, we regularly assist customers with impurity investigations performed either by the drug product manufacturer or another CRO. These cases...
Blog Post 9 – Through the Lens of GC/QTOF: Tracking Down Impurities in Ophthalmics 3 min reading time In the development of ophthalmic drug products, impurity profiling is essential to ensure long-term safety and regulatory compliance. While many impurities are...
