Abstract
To develop & validate new dissolution analytical method for venlafaxine in pellets by uv-spectrophotometer Solubility determination of venlafaxine in 0.1N HCl, Determine the absorption maxima of the drug in UV-Visible region in 0.1N HCl , Develop a new dissolution analytical method for venlafaxine in pellets by uv-spectrophotometer ,Validate the developed method as per ICH guidelines. The current good manufacturing practices (CGMP) and the Food Drug Administration (FDA) guidelines insist for adoption of sound methods of analysis with greater sensitivity and reproducibility. Therefore, the complexity of problems encountered in pharmaceutical analysis with the importance of achieving the selectivity, speed, low cost, simplicity, sensitivity, specificity, precision and accuracy in estimation of drugs.
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