ISBN: 9781441996305 - sample preparation of pharmaceutical dosage forms: challenges and strategies for sample preparation and extraction (21 risultati)

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  • Lingua: Inglese

    Editore: Springer, 2011

    1441996303 / 9781441996305

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  • Lingua: Inglese

    Editore: Springer, 2011

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  • Lingua: Inglese

    Editore: Springer, 2011

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    Condizione: New. pp. 412.

  • Lingua: Inglese

    Editore: Springer, 2011

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  • Lingua: Inglese

    Editore: Springer, 2011

    1441996303 / 9781441996305

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  • Lingua: Inglese

    Editore: Springer, 2011

    1441996303 / 9781441996305

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  • Lingua: Inglese

    Editore: Springer, 2011

    1441996303 / 9781441996305

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  • Lingua: Inglese

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    Da: California Books, Miami, FL, U.S.A.California Books

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  • Lingua: Inglese

    Editore: Springer, 2011

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    Da: Ria Christie Collections, Uxbridge, Regno UnitoRia Christie Collections

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    Condizione: New. In English.

  • Lingua: Inglese

    Editore: Springer, 2011

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

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    Buch. Condizione: Neu. Druck auf Anfrage Neuware - Printed after ordering - This book is intended to serve as a resource for analysts in developing and troubleshooting sample preparation methods. These are critical activities in providing accurate and reliable data throughout the lifecycle of a drug product. This book is divided into four parts:- Part One covers dosage form and diluent properties that impact sample preparation of pharmaceutical dosage forms and the importance of sampling considerations in generating data representative of the drug product batch. - Part Two reviews specific sample preparation techniques typically used with pharmaceutical dosage forms.- Part Three discusses sample preparation method development for different types of dosage forms including addressing drug excipient interactions and post extraction considerations, as well as method validation and applying Quality by Design (QbD) principles to sample preparation methods. - Part Four examines additional topics in sample preparation including automation, investigating aberrant potency results, green chemistry considerations for sample preparation and the ideal case where no sample preparation is required for sample analysis.…

  • Lingua: Inglese

    Editore: Springer US, 2011

    1441996303 / 9781441996305

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    Condizione: Sehr gut. Zustand: Sehr gut | Seiten: 412 | Sprache: Englisch | Produktart: Bücher | This book is intended to serve as a resource for analysts in developing and troubleshooting sample preparation methods.  These are critical activities in providing accurate and reliable data throughout the lifecycle of a drug product.  This book is divided into four parts:¿          Part One covers dosage form and diluent properties that impact sample preparation of pharmaceutical dosage forms and the importance of sampling considerations in generating data representative of the drug product batch.  ¿          Part Two reviews specific sample preparation techniques typically used with pharmaceutical dosage forms.¿          Part Three discusses sample preparation method development for different types of dosage forms including addressing drug excipient interactions and post extraction considerations, as well as method validation and applying Quality by Design (QbD) principles to sample preparation methods.   ¿          Part Four examines additional topics in sample preparation including automation, investigating aberrant potency results, green chemistry considerations for sample preparation and the ideal case where no sample preparation is required for sample analysis.…

  • Lingua: Inglese

    Editore: Springer US, 2011

    1441996303 / 9781441996305

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    Da: Buchpark, Trebbin, GermaniaBuchpark

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    Condizione: Sehr gut. Zustand: Sehr gut | Seiten: 412 | Sprache: Englisch | Produktart: Bücher | This book is intended to serve as a resource for analysts in developing and troubleshooting sample preparation methods.  These are critical activities in providing accurate and reliable data throughout the lifecycle of a drug product.  This book is divided into four parts:¿          Part One covers dosage form and diluent properties that impact sample preparation of pharmaceutical dosage forms and the importance of sampling considerations in generating data representative of the drug product batch.  ¿          Part Two reviews specific sample preparation techniques typically used with pharmaceutical dosage forms.¿          Part Three discusses sample preparation method development for different types of dosage forms including addressing drug excipient interactions and post extraction considerations, as well as method validation and applying Quality by Design (QbD) principles to sample preparation methods.   ¿          Part Four examines additional topics in sample preparation including automation, investigating aberrant potency results, green chemistry considerations for sample preparation and the ideal case where no sample preparation is required for sample analysis.…

  • Lingua: Inglese

    Editore: SPRINGER EXCLUSIVE(CBS), 2011

    1441996303 / 9781441996305

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    Condizione: New. Brand New! Fast Delivery This is an International Edition and ship within 24-48 hours. Deliver by FedEx and Dhl, & Aramex, UPS, & USPS and we do accept APO and PO BOX Addresses. Order can be delivered worldwide within 6-10 days and we do have flat rate for up to 2LB. Extra shipping charges will be requested if the Book weight is more than 5 LB. This Item May be shipped from India, United states & United Kingdom. Depending on your location and availability.…

  • Lingua: Inglese

    Editore: Springer, 2011

    1441996303 / 9781441996305

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    Da: Home-set, Mannheim, GermaniaHome-set

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    Gebundene Ausgabe. Condizione: Neu. This book is intended to serve as a resource for analysts in developing and troubleshooting sample preparation methods. These are critical activities in providing accurate and reliable data throughout the lifecycle of a drug product. This book is divided into four parts:? Part One covers dosage form and diluent properties that impact sample preparation of pharmaceutical dosage forms and the importance of sampling considerations in generating data representative of the drug product batch. ? Part Two reviews specific sample preparation techniques typically used with pharmaceutical dosage forms.? Part Three discusses sample preparation method development for different types of dosage forms including addressing drug excipient interactions and post extraction considerations, as well as method validation and applying Quality by Design (QbD) principles to sample preparation methods. ? Part Four examines additional topics in sample preparation including automation, investigating aberrant potency results, green chemistry considerations for sample preparation and the ideal case where no sample preparation is required for sample analysis. Sprache: Englisch Gewicht in Gramm: 729.…

  • Lingua: Inglese

    Editore: Springer, 2011

    1441996303 / 9781441996305

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  • Lingua: Inglese

    Editore: Springer Verlag, 2011

    1441996303 / 9781441996305

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    Hardcover. Condizione: Brand New. 1st edition. 397 pages. 9.75x6.50x1.00 inches. In Stock.

  • Lingua: Inglese

    Editore: Springer, 2011

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    Hardcover. Condizione: Like New. LIKE NEW. SHIPS FROM MULTIPLE LOCATIONS. book.

  • Lingua: Inglese

    Editore: Springer, 2011

    1441996303 / 9781441996305

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  • Lingua: Inglese

    Editore: Springer US, 2011

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    Gebunden. Condizione: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Volume focused entirely on sample preparation and extraction of pharmaceutical dosage formsA valuable resource in developing and troubleshooting sample preparation methods for drug products at all stages in the lifecycle of a drug productPr.…

  • Lingua: Inglese

    Editore: Springer US Aug 2011, 2011

    1441996303 / 9781441996305

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    Da: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, GermaniaBuchWeltWeit Ludwig Meier e.K.

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    Buch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -This book is intended to serve as a resource for analysts in developing and troubleshooting sample preparation methods. These are critical activities in providing accurate and reliable data throughout the lifecycle of a drug product. This book is divided into four parts:- Part One covers dosage form and diluent properties that impact sample preparation of pharmaceutical dosage forms and the importance of sampling considerations in generating data representative of the drug product batch. - Part Two reviews specific sample preparation techniques typically used with pharmaceutical dosage forms.- Part Three discusses sample preparation method development for different types of dosage forms including addressing drug excipient interactions and post extraction considerations, as well as method validation and applying Quality by Design (QbD) principles to sample preparation methods. - Part Four examines additional topics in sample preparation including automation, investigating aberrant potency results, green chemistry considerations for sample preparation and the ideal case where no sample preparation is required for sample analysis. 412 pp. Englisch.…

  • Lingua: Inglese

    Editore: Springer US, Springer US Aug 2011, 2011

    1441996303 / 9781441996305

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    Da: buchversandmimpf2000, Emtmannsberg, BAYE, Germaniabuchversandmimpf2000

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    Buch. Condizione: Neu. This item is printed on demand - Print on Demand Titel. Neuware -This book is intended to serve as a resource for analysts in developing and troubleshooting sample preparation methods. These are critical activities in providing accurate and reliable data throughout the lifecycle of a drug product.This book is divided into four parts:¿ Part One covers dosage form and diluent properties that impact sample preparation of pharmaceutical dosage forms and the importance of sampling considerations in generating data representative of the drug product batch.¿ Part Two reviews specific sample preparation techniques typically used with pharmaceutical dosage forms.¿ Part Three discusses sample preparation method development for different types of dosage forms including addressing drug excipient interactions and post extraction considerations, as well as method validation and applying Quality by Design (QbD) principles to sample preparation methods.¿ Part Four examines additional topics in sample preparation including automation, investigating aberrant potency results, green chemistry considerations for sample preparation and the ideal case where no sample preparation is required for sample analysis.Springer-Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg 412 pp. Englisch.…