Description
by
Jasmine Chaudhary (Author),
Akash Jain Shikha (Author),
Vipin Saini (Author)
Method development and validation of pharmaceutical dosage forms is a core area of quality control to assure the desired specifications in terms of strength, quality, purity, and identity of dosage form. The quality and safety of drugs can be maintained by estimating and monitoring the impurities effectively to assure that safe and effective drug formulations are available to consumers. High Performance Liquid Chromatography is the most versatile tool for the qualitative and quantitative analysis of drugs for analysis.
Number of Pages: 88Dimensions: 0.21 x 9 x 6 INPublication Date: May 15, 2021
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