The rate and extent of drug absorption are a function of many factors, including the site of administration, the physiochemical characteristics of the compound, and the dosage form. The issues involved in bioequivalence and bioavailability are enmeshed in controversy, which is compounded by issues o
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Editorial Reviews
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. . .recommended as a worthwhile library source for industry professionals.
---Pharmaceutical Technology
. . .industrial and governmental scientists will benefit from this book and library purchase is recommended.
---American Journal of Pharmaceutical Education
---Pharmaceutical Technology
. . .industrial and governmental scientists will benefit from this book and library purchase is recommended.
---American Journal of Pharmaceutical Education
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Inside This Book
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Key Phrases - Statistically Improbable Phrases (SIPs):
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uncomplicated drugs, bioequivalence regulations, enantioselective differences, physiological flow models, bioequivalence interval, vasoconstrictor test, effect compartment model, vivo bioequivalence study, bioavailability standards, bioequivalence standards, peroral dose, bioequivalence studies, active drug ingredient, bioequivalence issues, altered bioavailability, bioavailability parameters, bioequivalence requirements, therapeutic moiety, bioequivalence testing, bioequivalence data, such dosage forms, bioequivalence assessment, vivo bioavailability, bioequivalence problems, bioavailability studies Key Phrases - Capitalized Phrases (CAPs): (learn more)
New York, United States, Marcel Dekker, Raven Press, Drug Metab, European Community, Drug Dispos, Division of Bioequivalence, European Commission, Investigation of Bioavailability, Health Protection Branch, American Pharmaceutical Association, Office of Technology Assessment, Pharmacopeial Convention, Topical Therapeutic Products Workshop, Academic Press, Cosmetic Act, Meyer Figure, Pharmaceutical Manufacturers Association, Plenum Press, Council Directive, Drug Intelligence Publications, Drug Ref, Rate Extent Ref, Acta Med New!
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Front Cover | Table of Contents | First Pages | Index | Back Cover | Surprise Me!
uncomplicated drugs, bioequivalence regulations, enantioselective differences, physiological flow models, bioequivalence interval, vasoconstrictor test, effect compartment model, vivo bioequivalence study, bioavailability standards, bioequivalence standards, peroral dose, bioequivalence studies, active drug ingredient, bioequivalence issues, altered bioavailability, bioavailability parameters, bioequivalence requirements, therapeutic moiety, bioequivalence testing, bioequivalence data, such dosage forms, bioequivalence assessment, vivo bioavailability, bioequivalence problems, bioavailability studies Key Phrases - Capitalized Phrases (CAPs): (learn more)
New York, United States, Marcel Dekker, Raven Press, Drug Metab, European Community, Drug Dispos, Division of Bioequivalence, European Commission, Investigation of Bioavailability, Health Protection Branch, American Pharmaceutical Association, Office of Technology Assessment, Pharmacopeial Convention, Topical Therapeutic Products Workshop, Academic Press, Cosmetic Act, Meyer Figure, Pharmaceutical Manufacturers Association, Plenum Press, Council Directive, Drug Intelligence Publications, Drug Ref, Rate Extent Ref, Acta Med New!
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Front Cover | Table of Contents | First Pages | Index | Back Cover | Surprise Me!
Citations (learn more)
This book cites 86
books:
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86
books
cite this book:
See all 86 books citing this book
- Dermatological Formulations (Drugs and the Pharmaceutical Sciences) by B.w. Barry on 4 pages
- Physiology of the Gastrointestinal Tract, Fourth Edition (v. 1-2) by Kim E. Barrett on 4 pages
- Drug Absorption by Prescott on page 164, page 166, and page 416
- Percutaneous Absorption: Drugs, Cosmetics, Mechanisms, Methods, Fourth Edition (Drugs and the Pharmaceutical Sciences) by Robert L. Bronaugh on page 217, page 218, and page 219
- Modern Pharmaceutics by Gilbert S. Banker in Front Matter (1), Front Matter (2), and Front Matter (3)
See all 86 books this book cites
- Generics and Bioequivalence by Andre J. Jackson on 8 pages
- Development & Formulation of Veterinary Dosage Forms (Drugs and the Pharmaceutical Sciences) by Hardee on 6 pages
- Interspecies Pharmacokinetic Scaling: Principles And Application of Allometric Scaling by Iftekhar Mahmood on 4 pages
- Pharmacokinetics: Regulatory, Industrial, Academic Perspectives (Drugs and the Pharmaceutical Sciences) by Peter Welling in Front Matter, page 319, and page 405
- Cross-over Trials in Clinical Research (Statistics in Practice) by Stephen S Senn in Back Matter (1), Back Matter (2), and Back Matter (3)
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