Generic drug product development international regulatory requirements for bioequivalence
by
 
Kanfer, Isadore.

Title
Generic drug product development international regulatory requirements for bioequivalence

Author
Kanfer, Isadore.

ISBN
9781420020021

Publication Information
New York : Informa Healthcare USA, c2010.

Physical Description
xxi, 309 p. : ill.

Series
Drugs and the pharmaceutical sciences ; 201

Series Title
Drugs and the pharmaceutical sciences ; 201

Contents
1. Introduction / Isadore Kanfer -- 2. Australasia / C.T. Hung ... [et al.] -- 3. Brazil / Margareth R.C. Marques, Silvia Storpirtis, and Mr̀cia Martini Bueno -- 4. Canada / Iain J. McGilveray -- 5. European Union / Roger K. Verbeeck and Joelle Warlin -- 6. India / Subhash C. Mandal and S. Ravisankar -- 7. Japan / Juichi Riku -- 8. South Africa / Isadore Kanfer, Roderick B. Walker, and Michael F. Skinner -- 9. South America and Pan American Health Organization / Silvia Susana Giarcovich and Ricardo Bolaǫs -- 10. Taiwan / Li-Heng Pao, Jo-Feng Chi, and Oliver Yoa-Pu Hu -- 11. Turkey / Ilker Kanzik and A. Atilla Hincal -- 12. United States of America / Barbara M. Davit and Dale P. Connor -- 13. The World Health Organization / John D. Gordon ... [et al.].

Subject Term
Generic drugs.
 
Generic drugs -- Law and legislation.

Added Author
Kanfer, Isadore.
 
Shargel, Leon, 1941-

Electronic Access
Distributed by publisher. Purchase or institutional license may be required for access.


LibraryMaterial TypeItem BarcodeShelf Number[[missing key: search.ChildField.HOLDING]]Status
Online LibraryE-Book286727-1001ONLINEElektronik Kütüphane