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Añadir al carritoTaschenbuch. Condición: Neu. Impurity profiling in pharmaceuticals | "A Comprehensive Overview" | Mansi Jamdhade (u. a.) | Taschenbuch | Englisch | 2025 | LAP LAMBERT Academic Publishing | EAN 9786208435752 | Verantwortliche Person für die EU: SIA OmniScriptum Publishing, Brivibas Gatve 197, 1039 RIGA, LETTLAND, customerservice[at]vdm-vsg[dot]de | Anbieter: preigu.
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Añadir al carritoTaschenbuch. Condición: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Impurity profiling in pharmaceuticals refers to the process of identifying, characterizing, and quantifying any unwanted substances (impurities) present in a drug substance or drug product, which is crucial for ensuring safety and efficacy by monitoring and controlling their levels within acceptable regulatory limits; this involves using advanced analytical techniques to detect and analyze the structure of these impurities to assess potential toxicological risks. 52 pp. Englisch.
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Añadir al carritoPaperback. Condición: new. Paperback. Impurity profiling in pharmaceuticals refers to the process of identifying, characterizing, and quantifying any unwanted substances (impurities) present in a drug substance or drug product, which is crucial for ensuring safety and efficacy by monitoring and controlling their levels within acceptable regulatory limits; this involves using advanced analytical techniques to detect and analyze the structure of these impurities to assess potential toxicological risks. This item is printed on demand. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability.
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Añadir al carritoTaschenbuch. Condición: Neu. This item is printed on demand - Print on Demand Titel. Neuware -Impurity profiling in pharmaceuticals refers to the process of identifying, characterizing, and quantifying any unwanted substances (impurities) present in a drug substance or drug product, which is crucial for ensuring safety and efficacy by monitoring and controlling their levels within acceptable regulatory limits; this involves using advanced analytical techniques to detect and analyze the structure of these impurities to assess potential toxicological risks.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 52 pp. Englisch.
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Añadir al carritoTaschenbuch. Condición: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Impurity profiling in pharmaceuticals refers to the process of identifying, characterizing, and quantifying any unwanted substances (impurities) present in a drug substance or drug product, which is crucial for ensuring safety and efficacy by monitoring and controlling their levels within acceptable regulatory limits; this involves using advanced analytical techniques to detect and analyze the structure of these impurities to assess potential toxicological risks.