Method Development Validation Drugs by Dubey Som (6 results)

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Taschenbuch. Condition: Neu. Method Development & Validation Of Drugs By Chromatographic Technique | Pharmaceutical Chemistry | Som Shankar Dubey (u. a.) | Taschenbuch | 172 S. | Englisch | 2020 | LAP LAMBERT Academic Publishing | EAN 9786200533234 | Verantwortliche Person für die EU: BoD - Books on Demand, In de Tarpen 42, 22848 Norderstedt, info[at]bod[dot]de | Anbieter: preigu.

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Taschenbuch. Condition: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -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. 172 pp. Englisch.

Taschenbuch. Condition: Neu. This item is printed on demand - Print on Demand Titel. Neuware -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.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 172 pp. Englisch.

Taschenbuch. Condition: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - 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.