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Good Research Practice in Non-Clinical Pharmacology and Biomedicine
other
Editor(s):
Anton Bespalov
,
Martin C. Michel
,
Thomas Steckler
Publication date
(Print):
2020
Publisher:
Springer International Publishing
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There is no author summary for this book yet. Authors can add summaries to their books on ScienceOpen to make them more accessible to a non-specialist audience.
Related collections
Chinese General Practice
Author and book information
Book
ISBN (Print):
978-3-030-33655-4
ISBN (Electronic):
978-3-030-33656-1
Publication date (Print):
2020
DOI:
10.1007/978-3-030-33656-1
SO-VID:
c1f5c9f0-f617-41c3-a374-d7580c29f0e5
License:
https://creativecommons.org/licenses/by/4.0
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Book chapters
pp. 1
Quality in Non-GxP Research Environment
pp. 19
Guidelines and Initiatives for Good Research Practice
pp. 35
Learning from Principles of Evidence-Based Medicine to Optimize Nonclinical Research Practices
pp. 55
General Principles of Preclinical Study Design
pp. 71
Resolving the Tension Between Exploration and Confirmation in Preclinical Biomedical Research
pp. 81
Blinding and Randomization
pp. 101
Out of Control? Managing Baseline Variability in Experimental Studies with Control Groups
pp. 119
Quality of Research Tools
pp. 147
Genetic Background and Sex: Impact on Generalizability of Research Findings in Pharmacology Studies
pp. 163
Building Robustness into Translational Research
pp. 177
Minimum Information and Quality Standards for Conducting, Reporting, and Organizing In Vitro Research
pp. 197
Minimum Information in In Vivo Research
pp. 223
A Reckless Guide to P-values
pp. 257
Electronic Lab Notebooks and Experimental Design Assistants
pp. 277
Data Storage
pp. 299
Design of Meta-Analysis Studies
pp. 319
Publishers’ Responsibilities in Promoting Data Quality and Reproducibility
pp. 349
Quality Governance in Biomedical Research
pp. 367
Good Research Practice: Lessons from Animal Care and Use
pp. 383
Research Collaborations and Quality in Research: Foes or Friends?
pp. 399
Costs of Implementing Quality in Research Practice
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