Generic Drug Product Development: Specialty Dosage Forms

1st Edition

Leon Shargel, Isadore Kanfer

CRC Press
December 20, 2019 Forthcoming
Reference - 288 Pages
ISBN 9780367384395 - CAT# K450339

For Instructors Request Inspection Copy

was $74.95

USD$59.96

SAVE ~$14.99

Availabe for Pre-Order. This item will ship after December 20, 2019
Add to Wish List
FREE Standard Shipping!

Summary

Generic Drug Product Development: Specialty Dosage Forms explores the issues related to providing evidence of pharmaceutical equivalence and bioequivalence for specialty drug products. It describes various scientific approaches and regulatory requirements for manufacturers who need to demonstrate the therapeutic equivalence of generic specialty drug products to brand name alternatives.



The contributors discuss measurement of drug product quality and performance, as well as the regulatory and scientific requirements of topical, nasal and inhalation, and transdermal drug delivery products, along with generic biologics and modified release parenteral drug products.



The book is essential reading for specialists and researchers in pharmaceutical drug development, regulation, manufacturing, and others in the pharmaceutical sciences.

Instructors

We provide complimentary e-inspection copies of primary textbooks to instructors considering our books for course adoption.

Request an
e-inspection copy

Share this Title