Editors:
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
Part of the book series: Handbook of Experimental Pharmacology (HEP, volume 257)
Buying options
Table of contents (21 chapters)
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Front Matter
About this book
Keywords
- reproducibility
- study design
- data analysis
- data reporting
- data integrity
- quality management
- open access
Editors and Affiliations
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Partnership for Assessment & Accreditation of Scientific Practice, Heidelberg, Germany
Anton Bespalov
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Department of Pharmacology, Johannes Gutenberg University, Mainz, Germany
Martin C. Michel
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Janssen Pharmaceutica N.V., Beerse, Belgium
Thomas Steckler
Bibliographic Information
Book Title: Good Research Practice in Non-Clinical Pharmacology and Biomedicine
Editors: Anton Bespalov, Martin C. Michel, Thomas Steckler
Series Title: Handbook of Experimental Pharmacology
DOI: https://doi.org/10.1007/978-3-030-33656-1
Publisher: Springer Cham
eBook Packages: Biomedical and Life Sciences, Biomedical and Life Sciences (R0)
Copyright Information: The Editor(s) (if applicable) and The Author(s) 2020
License: CC BY
Hardcover ISBN: 978-3-030-33655-4Published: 21 February 2020
Softcover ISBN: 978-3-030-33658-5Published: 11 September 2020
eBook ISBN: 978-3-030-33656-1Published: 20 February 2020
Series ISSN: 0171-2004
Series E-ISSN: 1865-0325
Edition Number: 1
Number of Pages: X, 423
Number of Illustrations: 13 b/w illustrations, 21 illustrations in colour
Topics: Pharmacology, Neuroscience, Cardiology, Oncology