Good Research Practice in Non-Clinical Pharmacology and Biomedicine
Editors: Bespalov, Anton, Michel, Martin C., Steckler, Thomas (Eds.)
Free Preview- First comprehensive book on factors associated with high risk for poor reproducibility of non-clinical findings
- Inclusion of aspects of study design, data analysis and data reporting
- Broad applicability to in vitro and in vivo research across all therapeutic areas
- Open access
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- About this book
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This open access book, published under a CC BY 4.0 license in the Pubmed indexed book series Handbook of Experimental Pharmacology, provides up-to-date information on best practice to improve experimental design and quality of research in non-clinical pharmacology and biomedicine.
- Table of contents (21 chapters)
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Quality in Non-GxP Research Environment
Pages 1-17
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Guidelines and Initiatives for Good Research Practice
Pages 19-34
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Learning from Principles of Evidence-Based Medicine to Optimize Nonclinical Research Practices
Pages 35-54
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General Principles of Preclinical Study Design
Pages 55-69
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Resolving the Tension Between Exploration and Confirmation in Preclinical Biomedical Research
Pages 71-79
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Table of contents (21 chapters)
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Bibliographic Information
- Bibliographic Information
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- Book Title
- Good Research Practice in Non-Clinical Pharmacology and Biomedicine
- Editors
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- Anton Bespalov
- Martin C. Michel
- Thomas Steckler
- Series Title
- Handbook of Experimental Pharmacology
- Series Volume
- 257
- Copyright
- 2020
- Publisher
- Springer International Publishing
- Copyright Holder
- The Editor(s) (if applicable) and The Author(s)
- eBook ISBN
- 978-3-030-33656-1
- DOI
- 10.1007/978-3-030-33656-1
- Hardcover ISBN
- 978-3-030-33655-4
- Softcover ISBN
- 978-3-030-33658-5
- Series ISSN
- 0171-2004
- Edition Number
- 1
- Number of Pages
- X, 423
- Number of Illustrations
- 13 b/w illustrations, 21 illustrations in colour
- Topics
