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Generic Drug Product Development

Specialty Dosage Forms

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Pages
288 pages
Reading time
11 hours

More about the book

Focusing on pharmaceutical equivalence and bioequivalence, this volume addresses the scientific and regulatory challenges faced by manufacturers of specialty drug products. It outlines the necessary approaches to demonstrate therapeutic equivalence between generic and brand-name drugs. Additionally, the book covers the assessment of drug product quality and performance, emphasizing the regulatory requirements for various delivery methods, including topical, nasal, inhalation, transdermal, as well as generic biologics and modified release parenteral products.

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Generic Drug Product Development, Leon Shargel, Isadore Kanfer

Language
Released
2010
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