Handbook of Experimental Pharmacology
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Good Research Practice in Non-Clinical Pharmacology and Biomedicine

Editors: Bespalov, Anton, Michel, Martin C., Steckler, Thomas (Eds.)

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  • 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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eBook  
  • ISBN 978-3-030-33656-1
  • This book is an open access book, you can download it for free on link.springer.com
Hardcover 51,99 €
price for Spain (gross)
  • ISBN 978-3-030-33655-4
  • Free shipping for individuals worldwide
  • Institutional customers should get in touch with their account manager
  • Covid-19 shipping restrictions
  • Usually ready to be dispatched within 3 to 5 business days, if in stock
  • The final prices may differ from the prices shown due to specifics of VAT rules
Softcover 51,99 €
price for Spain (gross)
  • ISBN 978-3-030-33658-5
  • Free shipping for individuals worldwide
  • Institutional customers should get in touch with their account manager
  • Covid-19 shipping restrictions
  • Usually ready to be dispatched within 3 to 5 business days, if in stock
  • The final prices may differ from the prices shown due to specifics of VAT rules
About this book

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)

Table of contents (21 chapters)
  • Quality in Non-GxP Research Environment

    Pages 1-17

    Bongiovanni, Sandrine (et al.)

  • Guidelines and Initiatives for Good Research Practice

    Pages 19-34

    Kabitzke, Patricia (et al.)

  • Learning from Principles of Evidence-Based Medicine to Optimize Nonclinical Research Practices

    Pages 35-54

    Lefevre, Isabel A. (et al.)

  • General Principles of Preclinical Study Design

    Pages 55-69

    Huang, Wenlong (et al.)

  • Resolving the Tension Between Exploration and Confirmation in Preclinical Biomedical Research

    Pages 71-79

    Dirnagl, Ulrich

Buy this book

eBook  
  • ISBN 978-3-030-33656-1
  • This book is an open access book, you can download it for free on link.springer.com
Hardcover 51,99 €
price for Spain (gross)
  • ISBN 978-3-030-33655-4
  • Free shipping for individuals worldwide
  • Institutional customers should get in touch with their account manager
  • Covid-19 shipping restrictions
  • Usually ready to be dispatched within 3 to 5 business days, if in stock
  • The final prices may differ from the prices shown due to specifics of VAT rules
Softcover 51,99 €
price for Spain (gross)
  • ISBN 978-3-030-33658-5
  • Free shipping for individuals worldwide
  • Institutional customers should get in touch with their account manager
  • Covid-19 shipping restrictions
  • Usually ready to be dispatched within 3 to 5 business days, if in stock
  • The final prices may differ from the prices shown due to specifics of VAT rules
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Bibliographic Information

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
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