Liquid chromatography pharmaceutical development (3 risultati)

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  • Lingua: Inglese

    Editore: Aster Pub Corp, 1985

    0943330114 / 9780943330112

    • Rilegato

    Da: Zubal-Books, Since 1961, Cleveland, OH, U.S.A.Zubal-Books, Since 1961

    Venditore con 5 stelle
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    Condizione: Usato - Buono

    EUR 53,54

    EUR 3,92 spedizione 
    Spedito in U.S.A.

    Quantità: 1 disponibili

    Condizione: Good. 496 pp., Hardcover, ex library, front cover discolored else text clean and binding tight. - If you are reading this, this item is actually (physically) in our stock and ready for shipment once ordered. We are not bookjackers. Buyer is responsible for any additional duties, taxes, or fees required by recipient's country.

  • Condizione: Nuovo

    EUR 66,50

    EUR 70,00 spedizione 
    Spedito da Germania a U.S.A.

    Quantità: 5 disponibili

    Taschenbuch. Condizione: Neu. Analytical Method development by Liquid Chromatography | Development and Validation of Analytical Methods for the Assay of Selected Drugs in Pharmaceutical Dosage forms and Biological fluids | Prafulla Kumar Sahu (u. a.) | Taschenbuch | 352 S. | Englisch | 2011 | LAP LAMBERT Academic Publishing | EAN 9783844328691 | Verantwortliche Person für die EU: BoD - Books on Demand, In de Tarpen 42, 22848 Norderstedt, info[at]bod[dot]de | Anbieter: preigu.

  • Lingua: Inglese

    Editore: LAP LAMBERT Academic Publishing, 2011

    3844328696 / 9783844328691

    • Brossura
    • Print on Demand

    Da: AHA-BUCH GmbH, Einbeck, GermaniaAHA-BUCH GmbH

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    Condizione: Nuovo

    EUR 79,00

    EUR 62,71 spedizione 
    Spedito da Germania a U.S.A.

    Quantità: 1 disponibili

    Taschenbuch. Condizione: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Analytical methods development and validation play important roles in the discovery, development, and manufacture of pharmaceuticals. The current good manufacturing practice (cGMP) and Food Drug Administration (FDA) Guidelines insist for adoption of sound methods of analysis with greater sensitivity and reproducibility. This thesis describes analytical methods developed for drug determination in pharmaceutical dosage forms and biological matrixes including Chromatography (RP-HPLC) and Hyphenated Techniques (LC-MS/MS). Methods have been developed for separation and quantification of selected drugs from categories like Antihypertensive, Antihyperlipidemic, Skeletal Muscle Relaxant, Non-Steroidal Anti-inflammatory Drug (NSAID), Antibiotic, Anticonvulsant, Antiviral, and Analeptic.