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portada Method Development & Validation Of Drugs By Chromatographic Technique
Type
Physical Book
Author
Publisher
Language
English
Pages
172
Format
Paperback
Dimensions
22.9 x 15.2 x 1.0 cm
Weight
0.26 kg.
ISBN13
9786200533234
Categories

Method Development & Validation Of Drugs By Chromatographic Technique

Som Shankar Dubey (Author) · Mahesh Duggirala (Author) · LAP Lambert Academic Publishing · Paperback

Method Development & Validation Of Drugs By Chromatographic Technique - Dubey, Som Shankar ; Duggirala, Mahesh

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Synopsis "Method Development & Validation Of Drugs By Chromatographic Technique"

In the pharmaceutical industry, the quality control and quality assurance play major role in bringing out a safe and effective drug or dosage form. The pharmaceutical industry has delivered market safe, efficacious product that fulfills medical needs of the public.Development of new analytical methods for the determination of drugs quantitatively and qualitatively in pharmaceutical dosage forms is more important in pharmacokinetics, toxicological and biological studies. 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. Pharmaceutical analysis occupies a pivotal role in statuary certification of drugs and their formulations either by the industry or by the regulatory authorities. 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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