| 書名 | 作者 | 出版年 | 查看 | 回報錯誤連結 |
|---|
| Handbook of SOPs for good clinical practice |
Celine Clive. |
2004 |
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|
回報問題連結 |
| Design and analysis of clinical trials:concepts and methodologies / |
Shein-Chung Chow, Jen-Pei Liu. |
2014 |
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|
回報問題連結 |
| Physician investigator handbook:GCP tools and techniques / |
Deborah Rosenbaum, Fred Smith. |
2001 |
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|
回報問題連結 |
| Multiple analyses in clinical trials:fundamentals for investigators / |
Lemuel A. Moye. |
2003 |
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|
回報問題連結 |
| Methods and applications of statistics in clinical trials |
N. Balakrishnan. |
2014 |
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|
回報問題連結 |
| A practical guide to quality management in clinical trial research |
Graham D. Ogg. |
2006 |
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|
回報問題連結 |
| Design and analysis of clinical trials with time-to-event endpoints |
Karl E. Peace. |
2009 |
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|
回報問題連結 |
| An insider's guide to clinical trials |
Curtis L. Meinert. |
2011 |
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|
回報問題連結 |
| Clinical trials of antidepressants :how changing the model can uncover new, more effective molecules / |
Martin M. Katz. |
|
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|
回報問題連結 |
| Concepts, principles, trials, and design |
N. Balakrishnan. |
2014 |
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| Clinical research in Asia:opportunities and challenges / |
Umakanta Sahoo. |
2012 |
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|
回報問題連結 |
| Cancer clinical trials:current and controversial issues in design and analysis / |
Stephen L. George, Xiaofei Wang, Herbert Pang. |
2016 |
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|
回報問題連結 |
| Clinical trials:study design, endpoints and biomarkers, drug safety, FDA and ICH guidelines / |
Tom Brody. |
2012 |
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|
回報問題連結 |
| Clinical trials with missing data:a guide for practitioners / |
Michael O'Kelly, Bohdana Ratitch. |
2014 |
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|
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| Planning Clinical Research / |
Robert A. Parker, Nancy G. Berman. |
|
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|
回報問題連結 |
| Success probability estimation with applications to clinical trials |
Daniele De Martini. |
2013 |
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回報問題連結 |
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