Learn about intriguing findings from work with USP Chapter <1469>, Procedure 1, and a successful implementation of Procedure 3.
In compliance with USFDA requirements, these application notes describe the quantitation of nitrosamines in drugs and solvents using LC/MS or GC/MS.
Webinar case study of risk assessment implementation covering analytical methodologies for N-nitrosamines with their challenges and suggested solutions.
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