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Generic drug product development international regulatory requirements for bioequivalence için kapak resmi
Başlık:
Generic drug product development international regulatory requirements for bioequivalence
Yazar:
Kanfer, Isadore.
ISBN:
9781420020021
Yayın Bilgileri:
New York : Informa Healthcare USA, c2010.
Fiziksel Tanımlama:
xxi, 309 p. : ill.
Seri:
Drugs and the pharmaceutical sciences ; 201
Seri Başlığı:
Drugs and the pharmaceutical sciences ; 201
İçerik:
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.].
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