Vendeur : BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Allemagne
Taschenbuch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Determination of exact quantity of drug in the drug formulation requires accurate and robust analytical method. Analytical method development and validation plays an important role in the drug discovery, development, and quality control of pharmaceutical products. The method should be simple and fast so that it can be adopted by any laboratory easily. The methods which are used in analysis of stability studies for assay and related substances should be stability indicating analytical methods. The peaks of solutes and impurities under determination should be pure and hence peak purity in the methods for determination of assay and related impurities should be passed. The developed methods need to be validated as per current regulatory guidelines. All the validated methods should pass the acceptance criteria as per industrial and regulatory norms.Due to these high expectations, pharma industry is suffering, since many of the firms are using regular conventional techniques to determine the drug quantities and their impurities. To keep the pace with rapid improvement in quality standards of drugs all over the world and keeping in view the essential requirements. 160 pp. Englisch. N° de réf. du vendeur 9786139458653
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Vendeur : moluna, Greven, Allemagne
Etat : New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Mane DhananjayDr. Dhananjay Mane is presently working as a Professor & Director,YCM Open University . He has vast teaching and research experience . He has published so far 10 Reference books and 92 Research papers at international . N° de réf. du vendeur 385859452
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Vendeur : preigu, Osnabrück, Allemagne
Taschenbuch. Etat : Neu. Methods For Determinations Of Drugs, Drug Release & Its Impurities | Dhananjay Mane (u. a.) | Taschenbuch | 160 S. | Englisch | 2019 | LAP LAMBERT Academic Publishing | EAN 9786139458653 | Verantwortliche Person für die EU: BoD - Books on Demand, In de Tarpen 42, 22848 Norderstedt, info[at]bod[dot]de | Anbieter: preigu. N° de réf. du vendeur 116083226
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Vendeur : buchversandmimpf2000, Emtmannsberg, BAYE, Allemagne
Taschenbuch. Etat : Neu. This item is printed on demand - Print on Demand Titel. Neuware -Determination of exact quantity of drug in the drug formulation requires accurate and robust analytical method. Analytical method development and validation plays an important role in the drug discovery, development, and quality control of pharmaceutical products. The method should be simple and fast so that it can be adopted by any laboratory easily. The methods which are used in analysis of stability studies for assay and related substances should be stability indicating analytical methods. The peaks of solutes and impurities under determination should be pure and hence peak purity in the methods for determination of assay and related impurities should be passed. The developed methods need to be validated as per current regulatory guidelines. All the validated methods should pass the acceptance criteria as per industrial and regulatory norms.Due to these high expectations, pharma industry is suffering, since many of the firms are using regular conventional techniques to determine the drug quantities and their impurities. To keep the pace with rapid improvement in quality standards of drugs all over the world and keeping in view the essential requirements.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 160 pp. Englisch. N° de réf. du vendeur 9786139458653
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Vendeur : AHA-BUCH GmbH, Einbeck, Allemagne
Taschenbuch. Etat : Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Determination of exact quantity of drug in the drug formulation requires accurate and robust analytical method. Analytical method development and validation plays an important role in the drug discovery, development, and quality control of pharmaceutical products. The method should be simple and fast so that it can be adopted by any laboratory easily. The methods which are used in analysis of stability studies for assay and related substances should be stability indicating analytical methods. The peaks of solutes and impurities under determination should be pure and hence peak purity in the methods for determination of assay and related impurities should be passed. The developed methods need to be validated as per current regulatory guidelines. All the validated methods should pass the acceptance criteria as per industrial and regulatory norms.Due to these high expectations, pharma industry is suffering, since many of the firms are using regular conventional techniques to determine the drug quantities and their impurities. To keep the pace with rapid improvement in quality standards of drugs all over the world and keeping in view the essential requirements. N° de réf. du vendeur 9786139458653
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Vendeur : Revaluation Books, Exeter, Royaume-Uni
Paperback. Etat : Brand New. 160 pages. 8.66x5.91x0.37 inches. In Stock. N° de réf. du vendeur zk613945865X
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