| 書名 | 作者 | 出版年 | 查看 | 回報錯誤連結 |
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| Generic drug product development:solid oral dosage forms / |
Leon Shargel, Isadore Kanfer. |
2014 |
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|
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| Drug safety evaluation |
Shayne Cox Gad. |
2017 |
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|
回報問題連結 |
| Process scale purification of antibodies |
Uwe Gottschalk. |
2017 |
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|
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| How to validate a pharmaceutical process / |
Steven A. Ostrove. |
|
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|
回報問題連結 |
| How to develop robust solid oral dosage forms :from conception to post-approval / |
Bhavishya Mittal. |
|
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|
回報問題連結 |
| Pharmaceutical process chemistry for synthesis:rethinking the routes to scale-up / |
Peter J. Harrington. |
2011 |
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|
回報問題連結 |
| Fragment-based drug discovery:lessons and outlook / |
Daniel A. Erlanson and Wolfgang Jahnke. |
2016 |
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|
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| Drug-like properties :concepts, structure design and methods from ADME to toxicity optimization / |
Li Di and Edward H. Kerns. |
|
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| Biotechnology and biopharmaceuticals:transforming proteins and genes into drugs / |
Rodney J.Y. Ho and Milo Gibaldi. |
2013 |
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|
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| Evaluation of enzyme inhibitors in drug discovery:a guide for medicinal chemists and pharmacologists / |
Robert A. Copeland. |
2013 |
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|
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| Development and evaluation of drugs:from laboratory through licensure to market / |
Chi-Jen Lee, Lucia H. Lee, Cheng-Hsiung Lu. |
2003 |
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|
回報問題連結 |
| Drug discovery strategies and methods |
Alexandros Makriyannis, Diane Biegel. |
2004 |
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|
回報問題連結 |
| Pharmaceutical and medical applications of near-infrared spectroscopy |
Emil W. Ciurczak, James K. Drennen, III. |
2002 |
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|
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| Facility validation:theory, practice, and tools / |
Graham C. Wrigley. |
2004 |
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|
回報問題連結 |
| Isolation technology:a practical guide / |
Tim Coles. |
2004 |
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|
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| Fluid sterilization by filtration |
Peter R. Johnston. |
2003 |
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