Abstract:
The aim of this study was to statistically validate a spectrophotometric method for the quantification of paracetamol at a dosage of 1000 mg per tablet, based on internationally recognized analytical validation standards. Key parameters such as linearity, precision, accuracy, repeatability, and specificity were rigorously evaluated. The results demonstrated that the method exhibited satisfactory performance and complied with regulatory requirements.
The findings confirmed that the developed spectrophotometric method is statistically valid, showing a strong linear correlation (R² > 0.99) between absorbance and paracetamol concentration. This method is simple, fast, cost-effective, and efficient, making it well suited for quality control of paracetamol in pharmaceutical formulations.
