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Computational clusters have long provided a mechanism for the acceleration of high performance computing (HPC) applications. This book addresses the issue of fault-tolerance through checkpointing. It presents a general overview of checkpointing and how it'

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.