Generic Drug Product Development: International Regulatory Requirements for Bioequivalence

1st Edition

Isadore Kanfer, Isadore Kanfer, Leon Shargel, Leon Shargel

What are VitalSource eBooks?

CRC Press
Published April 19, 2016
Reference - 332 Pages
ISBN 9780429132919 - CAT# KE81968

For Instructors Request Inspection Copy

was $57.95

USD$52.16

SAVE ~$5.80

Add to Wish List
FREE Standard Shipping!

Summary

Due to a worldwide need for lower cost drug therapy, use of generic and multi-source drug products have been increasing. To meet international patent and trade agreements, the development and sale of these products must conform to national and international laws, and generic products must prove that they are of the same quality and are therapeutica

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