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Nitrosamine Drug Substance-Related Impurities (NDSRIs) have become one of the most critical topics in pharmaceutical quality, regulatory compliance, and nitrosamine risk assessment. These impurities are especially challenging because they originate from the drug molecule itself, making them harder to detect and control compared to traditional nitrosamine contaminants. In this video, you will learn everything you need to know about NDSRIs — what they are, how they form, why regulators like FDA and EMA are concerned, and how pharmaceutical companies perform risk assessment, testing, and control. Regulatory agencies now require manufacturers to perform risk assessments, confirmatory testing, and implement control strategies to keep NDSRI levels within acceptable limits to ensure patient safety. This video is especially useful for: Pharmaceutical professionals Analytical scientists Regulatory affairs professionals Quality assurance professionals Students preparing for pharma interviews Anyone working in Nitrosamine testing 📖 Read the detailed blog article: https://resolvemass.ca/ndsris-in-nitr... #Nitrosamine #NDSRI #NitrosamineTesting #PharmaceuticalAnalysis #LCMS #GenotoxicImpurities #PharmaQuality #RegulatoryAffairs #PharmaIndustry #AnalyticalChemistry #PharmaTraining #DrugSafety #FDA #PharmaEducation #ResolveMass