Generic Drug Product Development: Bioequivalence, International Regulatory Requirements, and Specialty Drug Products (Three-Volume Set)
by Leon Shargel;Isadore Kanfer (9781420063448)

Generic Drug Product Development: Bioequivalence, International Regulatory Requirements, and Specialty Drug Products (Three-Volume Set)
 
Leon Shargel;Isadore Kanfer
Release Date: 19 February 2010
Format: Hardcover
Pages: 288
Category: Pharmacology
ISBN: 9781420063448
ISBN-10: 1420063448



To be interchangeable with the brand name alternative, generic pharmaceutical products must demonstrate that they are its therapeutic equivalent. This title focuses on bioequivalence issues and alternate approaches to demonstrate bioequivalence of generic drugs. Exploring scientific, legal, and international regulatory challenges, this source discusses the use of alternative approaches to measure plasma drug concentrations for the demonstration of bioequivalence, and covers bioequivalence procedures for drug products that are not easily assessed based upon the chemical component of the drug.

AUD $373.95

 This title is not held in stock & is ordered from suppliers, subject to availability.


View other Leon Shargel;Isadore Kanfer titles like "Generic Drug Product Development: Bioequivalence, International Regulatory Requirements, and Specialty Drug Products (Three-Volume Set)"



Write a customer review of Generic Drug Product Development: Bioequivalence, International Regulatory Requirements, and Specialty Drug Products (Three-Volume Set).



If you like this title please tell others:

tell others

post to your Facebook wall post on Twitter post on Digg recommend to Stumbleupon bookmark on Delicious RSS feed send to a friend


Australian BookShop
Australian Bookshop. Established 2003
Search
Shopping Cart Customer Support


HolisticPage
International Online Store
of Inspiration
we ship everywhere
Australia Post
Australia Wide
.
Worldwide