Skills-based blogs, trainings and courses in pharmaceutical development
This article describes nitrosamine impurities in pharmaceuticals, their formation in the process, and their control strategies with case studies, and FAQs.
Impurities Control Strategies In Pharmaceuticals: Why & How Introduction and outcome: Impurities Control Strategies Impurities Control Strategies play a unique...
This article describes chromatographic peak integration, its types, interrelation errors and their source, and approaches to avoid integration errors with FAQs
Forced degradation studies reveal the intrinsic stability of pharmaceuticals, degradation pathways, and stability indicator strength of the analytical method.
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