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Good Research Practice in Non-Clinical Pharmacology and Biomedicine
Buch von Anton Bespalov (u. a.)
Sprache: Englisch

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Beschreibung
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.
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.
Zusammenfassung

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

Inhaltsverzeichnis
1. Quality in Non-GxP Research Environment.- 2. Guidelines & Initiatives for Good Research Practice.- 3. Learning from principles of evidence-based medicine to optimize nonclinical research practices.- 4. General Principles of Preclinical Study Design.- 5. Resolving the tension between exploration and confirmation in preclinical biomedical research.- 6. Blinding and Randomization.- 7. Out of control? Managing baseline variability in experimental studies with control groups.- 8. Quality of Research Tools.- 9. Genetic background and sex: impact on generalizability of research findings in pharmacology studies.- 10. Building robustness intro translational research.- 11. Minimum information and quality standards for conducting, reporting, and organizing in vitro research.- 12. Minimum Information in In Vivo Research.- 13. A reckless guide to P-values: Local evidence, global errors.- 14. Electronic Lab Notebooks and Experimental Design Assistants.- 15. Data storage.- 16. Design of meta-analysis studies.- 17. Publishers¿ responsibilities in promoting data quality and reproducibility.- 18. Quality governance in biomedical research.- 19. Good Research Practice ¿ Lessons from Animal Care & Use.- 20. Research collaborations and quality in research: foes or friends?.- 21. Costs of implementing quality in research practice.
Details
Erscheinungsjahr: 2020
Fachbereich: Toxikologie
Genre: Mathematik, Medizin, Naturwissenschaften, Technik
Rubrik: Wissenschaften
Medium: Buch
Inhalt: x
423 S.
13 s/w Illustr.
21 farbige Illustr.
423 p. 34 illus.
21 illus. in color.
ISBN-13: 9783030336554
ISBN-10: 3030336557
Sprache: Englisch
Einband: Gebunden
Autor: Bespalov, Anton
Michel, Martin C.
Steckler, Thomas
Redaktion: Bespalov, Anton
Steckler, Thomas
Michel, Martin C.
Herausgeber: Anton Bespalov/Martin C Michel/Thomas Steckler
Auflage: 1st edition 2020
Hersteller: Springer International Publishing
Verantwortliche Person für die EU: Springer Verlag GmbH, Tiergartenstr. 17, D-69121 Heidelberg, juergen.hartmann@springer.com
Maße: 241 x 160 x 29 mm
Von/Mit: Anton Bespalov (u. a.)
Erscheinungsdatum: 21.02.2020
Gewicht: 0,816 kg
Artikel-ID: 117457556
Zusammenfassung

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

Inhaltsverzeichnis
1. Quality in Non-GxP Research Environment.- 2. Guidelines & Initiatives for Good Research Practice.- 3. Learning from principles of evidence-based medicine to optimize nonclinical research practices.- 4. General Principles of Preclinical Study Design.- 5. Resolving the tension between exploration and confirmation in preclinical biomedical research.- 6. Blinding and Randomization.- 7. Out of control? Managing baseline variability in experimental studies with control groups.- 8. Quality of Research Tools.- 9. Genetic background and sex: impact on generalizability of research findings in pharmacology studies.- 10. Building robustness intro translational research.- 11. Minimum information and quality standards for conducting, reporting, and organizing in vitro research.- 12. Minimum Information in In Vivo Research.- 13. A reckless guide to P-values: Local evidence, global errors.- 14. Electronic Lab Notebooks and Experimental Design Assistants.- 15. Data storage.- 16. Design of meta-analysis studies.- 17. Publishers¿ responsibilities in promoting data quality and reproducibility.- 18. Quality governance in biomedical research.- 19. Good Research Practice ¿ Lessons from Animal Care & Use.- 20. Research collaborations and quality in research: foes or friends?.- 21. Costs of implementing quality in research practice.
Details
Erscheinungsjahr: 2020
Fachbereich: Toxikologie
Genre: Mathematik, Medizin, Naturwissenschaften, Technik
Rubrik: Wissenschaften
Medium: Buch
Inhalt: x
423 S.
13 s/w Illustr.
21 farbige Illustr.
423 p. 34 illus.
21 illus. in color.
ISBN-13: 9783030336554
ISBN-10: 3030336557
Sprache: Englisch
Einband: Gebunden
Autor: Bespalov, Anton
Michel, Martin C.
Steckler, Thomas
Redaktion: Bespalov, Anton
Steckler, Thomas
Michel, Martin C.
Herausgeber: Anton Bespalov/Martin C Michel/Thomas Steckler
Auflage: 1st edition 2020
Hersteller: Springer International Publishing
Verantwortliche Person für die EU: Springer Verlag GmbH, Tiergartenstr. 17, D-69121 Heidelberg, juergen.hartmann@springer.com
Maße: 241 x 160 x 29 mm
Von/Mit: Anton Bespalov (u. a.)
Erscheinungsdatum: 21.02.2020
Gewicht: 0,816 kg
Artikel-ID: 117457556
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