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)
Buy print copy
Tax calculation will be finalised at checkout
Table of contents (21 chapters)
-
Front Matter
Keywords
About this book
Editors and Affiliations
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
Industry Sectors: Biotechnology, Chemical Manufacturing, Consumer Packaged Goods, Health & Hospitals, Pharma