Generics Bioequivalence (9 results)

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    • Language: English

      Published by LAP LAMBERT Academic Publishing, 2013

      3659434515 / 9783659434518

      • Softcover

      Seller: Books Puddle, New York, NY, U.S.A.Books Puddle

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    • Language: English

      Published by CRC Press, 1994

      0849369304 / 9780849369308

      • Hardcover

      Seller: Mispah books, Redhill, SURRE, United KingdomMispah books

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      Hardcover. Condition: New. NEW. SHIPS FROM MULTIPLE LOCATIONS. book.

    • Language: English

      Published by CRC Press, 2020

      0367208318 / 9780367208318

      • Hardcover

      Seller: Buchpark, Trebbin, GermanyBuchpark

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      Condition: Gut. Zustand: Gut | Seiten: 203 | Sprache: Englisch | Produktart: Bücher | Keine Beschreibung verfügbar.

    • Language: English

      Published by LAP LAMBERT Academic Publishing Aug 2013, 2013

      3659434515 / 9783659434518

      • Softcover
      • Print on Demand

      Seller: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, GermanyBuchWeltWeit Ludwig Meier e.K.

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      Taschenbuch. Condition: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Bioavailability studies are used to define the effect of changes in the physicochemical properties of the drug substance and the effect of the drug product on the pharmacokinetics of the drug. Bioequivalence studies are used to compare the bioavailability of the same drug from various drug products. Bioavailability and bioequivalence can also be considered as performance measures of the drug product in-vivo. If the drug products are bioequivalent and therapeutically equivalent, then the clinical efficacy and the safety profile of these drug products are assumed to be similar and may be substituted for each other. If we ensure maximum bioavailability of a brand with a minimum production cost, it will be benefited for the patients in every aspect. So, comparative Bioavailabolity studies of various brands should be performed to establish a dosage regiment demonstrating evidence of safety and efficacy. 88 pp. Englisch.

    • Language: English

      Published by LAP LAMBERT Academic Publishing, 2013

      3659434515 / 9783659434518

      • Softcover
      • Print on Demand

      Seller: Majestic Books, Hounslow, United KingdomMajestic Books

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    • Language: English

      Published by LAP LAMBERT Academic Publishing, 2013

      3659434515 / 9783659434518

      • Softcover
      • Print on Demand

      Seller: moluna, Greven, Germanymoluna

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      Condition: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Al-Mamun Md. AbdullahCompleted post graduation at MS in Pharmaceutical Science from Jahangirnagar University, Bangladesh. Earlier studied Bachelor of Pharmacy at same university. Working as a Industrial Pharmacist (Executive, Product.

    • Language: English

      Published by LAP LAMBERT Academic Publishing, 2013

      3659434515 / 9783659434518

      • Softcover
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      Seller: Biblios, frankfurt am main, HESSE, GermanyBiblios

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    • Language: English

      Published by LAP LAMBERT Academic Publishing Aug 2013, 2013

      3659434515 / 9783659434518

      • Softcover
      • Print on Demand

      Seller: buchversandmimpf2000, Emtmannsberg, BAYE, Germanybuchversandmimpf2000

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      Taschenbuch. Condition: Neu. This item is printed on demand - Print on Demand Titel. Neuware -Bioavailability studies are used to define the effect of changes in the physicochemical properties of the drug substance and the effect of the drug product on the pharmacokinetics of the drug. Bioequivalence studies are used to compare the bioavailability of the same drug from various drug products. Bioavailability and bioequivalence can also be considered as performance measures of the drug product in-vivo. If the drug products are bioequivalent and therapeutically equivalent, then the clinical efficacy and the safety profile of these drug products are assumed to be similar and may be substituted for each other. If we ensure maximum bioavailability of a brand with a minimum production cost, it will be benefited for the patients in every aspect. So, comparative Bioavailabolity studies of various brands should be performed to establish a dosage regiment demonstrating evidence of safety and efficacy.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 88 pp. Englisch.

    • Language: English

      Published by LAP LAMBERT Academic Publishing, 2013

      3659434515 / 9783659434518

      • Softcover
      • Print on Demand

      Seller: AHA-BUCH GmbH, Einbeck, GermanyAHA-BUCH GmbH

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      Taschenbuch. Condition: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Bioavailability studies are used to define the effect of changes in the physicochemical properties of the drug substance and the effect of the drug product on the pharmacokinetics of the drug. Bioequivalence studies are used to compare the bioavailability of the same drug from various drug products. Bioavailability and bioequivalence can also be considered as performance measures of the drug product in-vivo. If the drug products are bioequivalent and therapeutically equivalent, then the clinical efficacy and the safety profile of these drug products are assumed to be similar and may be substituted for each other. If we ensure maximum bioavailability of a brand with a minimum production cost, it will be benefited for the patients in every aspect. So, comparative Bioavailabolity studies of various brands should be performed to establish a dosage regiment demonstrating evidence of safety and efficacy.