| 書名 | 作者 | 出版年 | 查看 | 回報錯誤連結 |
|---|
| Understanding drug release and absorption mechanisms:a physical and mathematical approach / |
Mario Grassi ... [et al.]. |
2007 |
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|
回報問題連結 |
| Drug safety evaluation |
Shayne Cox Gad. |
2017 |
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|
回報問題連結 |
| Drug Screening Methods:(Preclinical Evaluation of New Drugs) / |
SK Gupta. |
2009 |
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|
回報問題連結 |
| Safety pharmacology in pharmaceutical development and approval |
Shayne C. Gad. |
2004 |
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|
回報問題連結 |
| The process of new drug discovery and development |
Charles G. Smith, James T. O'Donnell. |
2006 |
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|
回報問題連結 |
| Smith and Williams' introduction to the principles of drug design and action |
H. John Smith. |
2006 |
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回報問題連結 |
| Assessing bioavailability of drug delivery systems:mathematical and numerical treatment / |
Jean-Maurice Vergnaud, Iosif-Daniel Rosca. |
2005 |
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|
回報問題連結 |
| Data and safety monitoring committees in clinical trials |
Jay Herson. |
2009 |
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|
回報問題連結 |
| Psychostimulants |
George F. Koob, Michael A. Arends, Mandy L. McCracken, Michel Le Moal. |
2020 |
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|
回報問題連結 |
| Pharmacological CLASSIFICATION OF DRUGS with Doses and Preparations |
KD Tripathi. |
2010 |
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|
回報問題連結 |
| A handbook of bioanalysis and drug metabolism |
Gary Evans. |
2004 |
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|
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| Hygiene in der arzneimittelproduktion :Sterile und nicht-sterile Arzeneiformen / |
Michael Rieth und Norbert Krämer. |
|
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|
回報問題連結 |
| ICH quality guidelines:an implementation guide / |
Andrew Teasdale, David Elder, Raymond W. Nims. |
2018 |
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|
回報問題連結 |
| Peptidomimetics in organic and medicinal chemistry:the art of transforming peptides in drugs / |
Andrea Trabocchi and Antonio Guarna. |
2014 |
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|
回報問題連結 |
| Simulation for designing clinical trials:a pharmacokinetic-pharmacodynamic modeling perspective / |
[edited by] Hui C. Kimko, Stephen B. Duffull. |
2003 |
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|
回報問題連結 |
| Modern pharmaceutics |
Gilbert S. Banker, Christopher T. Rhodes. |
2002 |
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回報問題連結 |
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