Validation of Stability using the Chromatography Method

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Many studies were depicted the development of a validated reversed-phase HPLC method for the determination of the primary drug in thepresence of degradation products or pharmaceutical excipients. The separation is carried out on Hypersil BDS C18 column having particle size 5 μ using acetate buffer.

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at https://www.scitechnol.com/peer-review/development-and-validation-of-stability-indicating-hplc-method-for-gefitinib-and-its-related-compounds-and-characterisation-of-deg-XlJY.php?article_id=5776

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