| 書名 | 作者 | 出版年 | 查看 | 回報錯誤連結 |
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| Essentials of pharmaceutical analysis / |
Muhammad Sajid Hamid Akash, Kanwal Rehman. |
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| Toxicology of nanoparticles :insights from drosophila / |
Namita Agrawal, Prasanna Shah. |
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| Analytical techniques in the pharmaceutical sciences |
Anette Mullertz, Yvonne Perrie, Thomas Rades. |
2016 |
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| Regulated bioanalysis:fundamentals and practice / |
Mario L. Rocci Jr., Stephen Lowes. |
2017 |
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| Drug Testing in Alternate Biological Specimens |
Amanda J. Jenkins, Yale H. Caplan. |
2008 |
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| Drugs and Poisons in Humans:A Handbook of Practical Analysis / |
[edited by] Osamu Suzuki, Kanako Watanabe. |
2005 |
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| Raman and SERS Investigations of Pharmaceuticals |
Monica Baia, Simion Astilean, Traian Iliescu. |
2008 |
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| High throughput bioanalytical sample preparation:methods and automation strategies / |
David A. Wells. |
2003 |
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| Benefit-risk assessment of medicines ::the development and application of a universal framework for decision-making and effective communication / |
James Leong, Sam Salek, Stuart Walker. |
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| Method validation in pharmaceutical analysis:a guide to best practice / |
Joachim Ermer and Phil Nethercote. |
2015 |
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| Preparative chromatography |
Henner Schmidt-Traub, Michael Schulte and Andreas Seidel-Morgenstern. |
2012 |
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| The essential guide to N-of-1 trials in health |
Jane Nikles, Geoffrey Mitchell. |
2015 |
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| Fine particles in medicine and pharmacy |
Egon Matijevic. |
2012 |
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| LC-MS in drug bioanalysis |
Q. Alan Xu, Timothy L. Madden. |
2012 |
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