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Good Research Practice in Non-Clinical Pharmacology and Biomedicine

  • Book
  • Open Access
  • © 2020

You have full access to this open access Book


  • 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

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.

Editors and Affiliations

  • Partnership for Assessment & Accreditation of Scientific Practice, Heidelberg, Germany

    Anton Bespalov

  • Department of Pharmacology, Johannes Gutenberg University, Mainz, Germany

    Martin C. Michel

  • Janssen Pharmaceutica N.V., Beerse, Belgium

    Thomas Steckler

Bibliographic Information

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