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I have an HPLC method for the analysis of impurities in API, do you think I can use the same method for the analysis of impurities and degradation products in Drug Product?
Thank you very much in advance
Discussions about HPLC, CE, TLC, SFC, and other "liquid phase" separation techniques.
Kina83 wrote:
And where to start? How to know what impurities can be generated? Can there be different impurities in the API than in the final product? How to fulfill the lCH? Thanks so much for any help
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