Analytical Method Validation for Drug Stability Analysis

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This presentation delves into the analytical validation of Tenofovir Disoproxil Fumarate (TDF), highlighting UV-visible spectroscopy's role in addressing stability challenges. A specific UV spectrophotometric method, developed and validated under ICH guidelines, examines niosomal formulations, ensuring precision and reliability. The experimental focus includes standard solution preparation and assessing pH-dependent degradation. Results showcase the method's high linearity and precision, with...