Overview
- 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)
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Table of contents(21 chapters)
About this book
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
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/Toxicology, Neurosciences, Cardiology, Oncology