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Generic Drug Product Development Bioequivalence Issues (HB)
Books from same Author: Kanfer
Books from same Publisher: Informa Healthcare

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Description

The assessment of bioequivalence is an important process whereby the bioavailability of a generic drug product is compared with its brand-name counterpart. Generic pharmaceutical products must be approved as therapeutic equivalents to the brand name alternative in order to be interchangeable. The demonstration of bioequivalence is an important component of therapeutic equivalence. Bioequivalence studies are very expensive, time consuming and always have the possibility of failure. The objective of this textbook is to describe some of those specific bioequivalence issues which need to be considered for the design and conduct of bioequivalence studies. By exploring scientific, legal, and international regulatory challenges, Generic Drug Development, discusses the use of alternative approaches to the measurement of plasma drug concentrations for the demonstration of bioequivalence, and covers bioequivalence procedures for drug products that are not easily assessed - based upon the physical and chemical properties of the active drug and the nature of the drug product.

More Details About Generic Drug Product Development Bioequivalence Issues (HB)
General Information
Author(s)Kanfer
PublisherInforma Healthcare
Edition1
ISBN9780849377846
Pages264
BindingHard Back
LanguageEnglish
Publish YearJanuary 2008
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