| 書名 | 作者 | 出版年 | 查看 | 回報錯誤連結 |
|---|
| Handbook of pharmaceutical manufacturing formulations. |
Sarfaraz K. Niazi. |
2009 |
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回報問題連結 |
| Handbook of pharmaceutical manufacturing formulations. |
Sarfaraz K. Niazi. |
2009 |
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|
回報問題連結 |
| Handbook of pharmaceutical manufacturing formulations. |
Sarfaraz K. Niazi. |
2009 |
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|
回報問題連結 |
| Handbook of pharmaceutical manufacturing formulations. |
Sarfaraz K. Niazi. |
2009 |
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|
回報問題連結 |
| Handbook of pharmaceutical manufacturing formulations. |
Sarfaraz K. Niazi. |
2009 |
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|
回報問題連結 |
| Preformulation in solid dosage form development |
Moji Christianah Adeyeye, Harry G. Brittain. |
2008 |
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|
回報問題連結 |
| Aqueous polymeric coatings for pharmaceutical dosage forms |
|
2008 |
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|
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| Generic drug product development:international regulatory requirements for bioequivalence / |
Isadore Kanfer, Leon Shargel. |
2010 |
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|
回報問題連結 |
| Generic drug product development:specialty dosage forms / |
Leon Shargel, Isadore Kanfer. |
2010 |
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|
回報問題連結 |
| Pharmaceutical pre-approval inspections:a guide to regulatory success / |
Martin D. Hynes III. |
2008 |
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|
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| Handbook of drug screening |
Ramakrishna Seethala, Litao Zhang. |
2009 |
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|
回報問題連結 |
| Polymorphism in pharmaceutical solids |
Harry G. Brittain. |
2009 |
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|
回報問題連結 |
| FDA regulatory affairs:a guide for prescription drugs, medical devices, and biologics / |
Douglas J. Pisano, David S. Mantus. |
2008 |
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|
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| International pharmaceutical product registration |
Anthony Cartwright, Brian R. Matthews. |
2009 |
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| Preclinical drug development |
Mark C. Rogge, David R. Taft. |
2010 |
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| Pharmaceutical process engineering |
Anthony J. Hickey, David Ganderton. |
2010 |
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|
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| Biodrug delivery systems:fundamentals, applications and clinical development / |
Mariko Morishita, Kinam Park. |
2010 |
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|
回報問題連結 |
| Active pharmaceutical ingredients:development, manufacturing, and regulation / |
Stanley H. Nusim. |
2010 |
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回報問題連結 |
| Handbook of pharmaceutical granulation technology |
Dilip M. Parikh. |
2010 |
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|
回報問題連結 |
| Handbook of pharmaceutical manufacturing formulations. |
Sarfaraz K. Niazi. |
2009 |
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|
回報問題連結 |
| Towards drugs of the future:key issues in lead finding and lead optimization / |
C.G. Kruse and H. Timmerman. |
2008 |
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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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回報問題連結 |
| How to validate a pharmaceutical process / |
Steven A. Ostrove. |
|
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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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|
回報問題連結 |
| 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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| 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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|
回報問題連結 |
| Fluid sterilization by filtration |
Peter R. Johnston. |
2003 |
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回報問題連結 |
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