Complete workflow for determining the content of nevirapine and related impurities

In both research and development and quality control pharmaceutical laboratories, determining the content of an active pharmaceutical ingredient (API) and its related impurities are typical analyses. While it is common to apply different methods for assay and impurity determination for one API, for instance in many pharmacopoeia monographs, in practice it is preferred to combine both analyses into one single run. Using a software assisted method development approach is hereby a very practical tool to speed up the method development process to save time and resources.