Systematic approach to develop and validate High Performance Liquid Chromatographic method for efavirenz and its degradants
Background: The crucial aspect to consider during method development and validation, ensuring accurate, precise, and specific estimation of drug substances and drug products, is stability. Various factors, including environmental, instrumental, reagent, and human factors, can pose challenges in achi...
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Creative Pharma Assent,
2024-06-01T00:00:00Z.
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