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Good Research Practice in Non-Clinical Pharmacology and Biomedicine

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Cover of 'Good Research Practice in Non-Clinical Pharmacology and Biomedicine'

Table of Contents

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    Book Overview
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    Chapter 274 Quality in Non-GxP Research Environment
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    Chapter 275 Guidelines and Initiatives for Good Research Practice
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    Chapter 276 Learning from Principles of Evidence-Based Medicine to Optimize Nonclinical Research Practices
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    Chapter 277 General Principles of Preclinical Study Design
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    Chapter 278 Resolving the Tension Between Exploration and Confirmation in Preclinical Biomedical Research
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    Chapter 279 Blinding and Randomization
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    Chapter 280 Out of Control? Managing Baseline Variability in Experimental Studies with Control Groups
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    Chapter 281 Quality of Research Tools
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    Chapter 282 Genetic Background and Sex: Impact on Generalizability of Research Findings in Pharmacology Studies
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    Chapter 284 Minimum Information and Quality Standards for Conducting, Reporting, and Organizing In Vitro Research.
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    Chapter 285 Minimum Information in In Vivo Research.
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    Chapter 286 A Reckless Guide to P-values
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    Chapter 288 Data Storage
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    Chapter 290 Publishers’ Responsibilities in Promoting Data Quality and Reproducibility
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    Chapter 291 Quality Governance in Biomedical Research
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    Chapter 292 Good Research Practice: Lessons from Animal Care and Use
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    Chapter 293 Research Collaborations and Quality in Research: Foes or Friends?
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    Chapter 294 Costs of Implementing Quality in Research Practice
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Title
Good Research Practice in Non-Clinical Pharmacology and Biomedicine
Published by
Springer International Publishing, January 2020
DOI 10.1007/978-3-030-33656-1
ISBNs
978-3-03-033655-4, 978-3-03-033656-1
Editors

Anton Bespalov, Martin C. Michel, Thomas Steckler

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