| 書名 | 作者 | 出版年 | 查看 | 回報錯誤連結 |
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| The science and regulations of naturally derived complex drugs / |
Ram Sasisekharan, Sau L. Lee, Amy Rosenberg, Larry A. Walker. |
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| Practical statistics for pharmaceutical analysis :with Minitab applications / |
James E. De Muth. |
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| Bioequivalence requirements in various global jurisdictions / |
Isadore Kanfer. |
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| Regulated bioanalysis:fundamentals and practice / |
Mario L. Rocci Jr., Stephen Lowes. |
2017 |
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| ADME processes in pharmaceutical sciences :dosage, design, and pharmacotherapy success / |
Alan Talevi, Pablo A. M. Quiroga. |
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| Dictionary of pharmaceutical medicine |
Gerhard Nahler. |
2017 |
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| Endotoxin detection and control in pharma, limulus, and mammalian systems / |
Kevin L. Williams. |
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| Translating molecules into medicines:cross-functional integration at the drug discovery-development interface / |
Shobha N. Bhattachar ... [et al.]. |
2017 |
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| New drug development:an introduction to clinical trials / |
J. Rick Turner. |
2010 |
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| FDA bioequivalence standards / |
Lawrence X. Yu, Bing V. Li. |
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| Applied pharmacometrics / |
Stephan Schmidt, Hartmut Derendorf. |
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| Discovering and developing molecules with optimal drug-like properties / |
Allen C Templeton, Stephen R. Byrn, Roy J Haskell, Thomas E. Prisinzano. |
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| Nanomedicine |
Kenneth A. Howard, Thomas Vorup-Jensen, Dan Peer. |
2016 |
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| Translating molecular biomarkers into clinical assays:techniques and applications / |
Russell Weiner, Marian Kelley. |
2016 |
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| Challenges in protein product development |
Nicholas W. Warne, Hanns-Christian Mahler. |
2018 |
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| Formulating poorly water soluble drugs |
Robert O. Williams III, Alan B. Watts, Dave A. Miller. |
2016 |
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