| 書名 | 作者 | 出版年 | 查看 | 回報錯誤連結 |
|---|
| Equipment qualification in the pharmaceutical industry |
Steven Ostrove. |
2019 |
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| Drug safety evaluation |
Shayne Cox Gad. |
2017 |
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|
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| Process scale purification of antibodies |
Uwe Gottschalk. |
2017 |
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|
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| Pharmaceutical process chemistry for synthesis:rethinking the routes to scale-up / |
Peter J. Harrington. |
2011 |
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|
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| Fragment-based drug discovery:lessons and outlook / |
Daniel A. Erlanson and Wolfgang Jahnke. |
2016 |
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|
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| How to develop robust solid oral dosage forms :from conception to post-approval / |
Bhavishya Mittal. |
|
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|
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| Trends in drug research III:proceedings of the 13th Noordwijkerhout-Caminero [sic] Symposium, the Netherlands, 6-11 May 2001 / |
Henk van der Goot. |
2002 |
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|
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| Handbook of isolation and characterization of impurities in pharmaceuticals |
Satinder Ahuja, Karen Mills Alsante. |
2003 |
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| High throughput analysis for early drug discovery |
James N. Kyranos. |
2004 |
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| Advances in medicinal chemistry. |
|
1999 |
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|
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| Advances in medicinal chemistry. |
|
2000 |
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|
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| Target validation in drug discovery |
editors, Brian W. Metcalf and Susan Dillon. |
2007 |
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|
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| Drug-like properties:concepts, structure design and methods : from ADME to toxicity optimization / |
Edward H. Kerns and Li Di. |
2008 |
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| Modified-release drug delivery technology. |
Michael J. Rathbone ... [et al.]. |
2008 |
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|
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| Modified-release drug delivery technology. |
Michael J. Rathbone ... [et al.]. |
2008 |
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|
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| Handbook of pharmaceutical manufacturing formulations. |
Sarfaraz K. Niazi. |
2009 |
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