| 書名 | 作者 | 出版年 | 查看 | 回報錯誤連結 |
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| Testing computer systems for FDA/MHRA compliance |
David Stokes. |
2004 |
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|
回報問題連結 |
| Equipment qualification in the pharmaceutical industry |
Steven Ostrove. |
2019 |
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|
回報問題連結 |
| Current research in pharmaceutical technology |
Sabine Globig, William Hunter. |
2011 |
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|
回報問題連結 |
| An introduction to pharmaceutical sciences:production, chemistry, techniques and technology / |
Jiben Roy. |
2011 |
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|
回報問題連結 |
| Applied case studies and solutions in molecular docking-based drug design |
Siavoush Dastmalchi, Tabriz University of Medical Sciences, Iran, Maryam Hamzeh-Mivehroud,Tabriz University of Medical Sciences, Iran, and Babak Sokouti, Tabriz University of Medical Sciences, Iran, editors. |
|
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|
回報問題連結 |
| Comprehensive quality by design for pharmaceutical product development and manufacture |
Gintaras V. Reklaitis, Christine Seymour, Salvador García-Munoz. |
2017 |
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|
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| Continuous manufacturing of pharmaceuticals |
Peter Kleinebudde, Johannes Khinast, Jukka Rantanen. |
2017 |
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|
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| Facility validation:theory, practice, and tools / |
Graham C. Wrigley. |
2004 |
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|
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| Pharmaceutical extrusion technology |
Isaac Ghebre-Sellassie, Charles Martin. |
2003 |
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|
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| Advanced pharmaceutics:physicochemical principles / |
Cherng-Ju Kim. |
2004 |
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|
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| Pharmaceutical engineering change control |
editor, Simon G. Turner. |
2004 |
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|
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| Good design practices for GMP pharmaceutical facilities |
Andrew A. Signore, Terry Jacobs. |
2005 |
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|
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| Pharmaceutical process scale-up |
Michael Levin. |
2006 |
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|
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| Validating pharmaceutical systems:good computer practice in life science manufacturing / |
John Andrews. |
2005 |
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|
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| Good laboratory practice regulations |
Sandy Weinberg. |
2003 |
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|
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| Theory and practice of contemporary pharmaceutics |
Tapash K. Ghosh, Bhaskara R. Jasti. |
2005 |
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