Generic drug product development : international regulatory requirements for bioequivalence
tarafından
Kanfer, Isadore.
Başlık
:
Generic drug product development : international regulatory requirements for bioequivalence
Yazar
:
Kanfer, Isadore.
ISBN
:
9780429132919
Fiziksel Tanımlama
:
1 online resource (xxi, 309 pages).
Seri
:
Drugs and the pharmaceutical sciences ; Volume 201
Drugs and the pharmaceutical sciences ; Volume 201.
İçerik
:
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.].
Konu Terimleri
:
Generic drugs.
Generic drugs -- Law and legislation.
Yazar Ek Girişi
:
Kanfer, Isadore.
Shargel, Leon, 1941-
Elektronik Erişim
:
| Kütüphane | Materyal Türü | Demirbaş Numarası | Yer Numarası | [[missing key: search.ChildField.HOLDING]] | Durumu/İade Tarihi |
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| Çevrimiçi Kütüphane | E-Kitap | 545952-1001 | RS55.2 .G454 2010 | | CRC E-Books |