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
9780429132919

Physical Description
1 online resource (xxi, 309 pages).

Series
Drugs and the pharmaceutical sciences ; Volume 201
 
Drugs and the pharmaceutical sciences ; Volume 201.

Contents
1. Introduction / Isadore Kanfer -- 2. Australasia / C.T. Hung. [et al.] -- 3. Brazil / Margareth R.C. Marques, Silvia Storpirtis, and Marcia 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 Bolanos -- 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
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LibraryMaterial TypeItem BarcodeShelf Number[[missing key: search.ChildField.HOLDING]]Status
Online LibraryE-Book545952-1001RS55.2 .G454 2010CRC E-Books