Generic drug product development = i...
Kanfer, Isadore.

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  • Generic drug product development = international regulatory requirements for bioequivalence /
  • 紀錄類型: 書目-電子資源 : Monograph/item
    正題名/作者: Generic drug product development/ edited by Isadore Kanfer, Leon Shargel.
    其他題名: international regulatory requirements for bioequivalence /
    其他作者: Kanfer, Isadore.
    出版者: New York :Informa Healthcare USA, : c2010.,
    面頁冊數: xxi, 309 p. :ill.
    內容註: 1. Introduction / Isadore Kanfer -- 2. Australasia / C.T. Hung ... [et al.] -- 3. Brazil / Margareth R.C. Marques, Silvia Storpirtis, and M�arcia 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 Bola�nos -- 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.].
    標題: Generic drugs. -
    電子資源: http://marc.crcnetbase.com/isbn/9781420020021Distributed by publisher. Purchase or institutional license may be required for access.
    ISBN: 9781420020021 (ebook : PDF)
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W9133267 電子資源 11.線上閱覽_V 電子書 EB RS55.2 .G454 2010 一般使用(Normal) 在架 0
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