Identifying and Quantifying Mutagenic Impurities in Pharmaceutical Products

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Identifying and Quantifying Mutagenic Impurities in Pharmaceutical Products

Published on: June 16, 2020

LCGC E-Books

LCGC E-Books, LCGC E-Books-07-20-2020, Issue 17

Pages: 17–26

Meeting detection challenges presented by nitrosamine impurities Determination of NDMA and nitrosamine impurities using triple-quadrupole LC/MS Determination of genotoxic impurities in ranitidine APIs and drug products