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The application of quality by design in the development of the liquid chromatography method to determine empagliflozin in the presence of its organic impurities
Analysis of impurities is an important step in the quality control of pharmaceutical ingredients and final products. From drug synthesis or excipients, even in small concentrations, impurities may affect efficacy and safety. The method was developed following Quality by Design (QbD) for the analysis...
| Autores principales: | , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
The Royal Society of Chemistry
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9049826/ https://www.ncbi.nlm.nih.gov/pubmed/35493885 http://dx.doi.org/10.1039/c9ra08442h |