Good Research Practice in Non-Clinical Pharmacology and Biomedicine / / edited by Anton Bespalov, Martin C. Michel, Thomas Steckler.
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.
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Superior document: | Handbook of Experimental Pharmacology, 257 |
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Place / Publishing House: | Cham : : Springer International Publishing :, Imprint: Springer,, 2020. |
Year of Publication: | 2020 |
Edition: | 1st ed. 2020. |
Language: | English |
Series: | Handbook of Experimental Pharmacology ;
257 |
Physical Description: | 1 online resource (X, 423 p. 34 illus., 21 illus. in color.) |
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(CKB)4100000010480154 (DE-He213)978-3-030-33656-1 (MiAaPQ)EBC6120896 (Au-PeEL)EBL6120896 (OCoLC)1143621169 (oapen)https://directory.doabooks.org/handle/20.500.12854/29538 (PPN)242976573 (EXLCZ)994100000010480154 |
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Bespalov, Anton edt Good Research Practice in Non-Clinical Pharmacology and Biomedicine / edited by Anton Bespalov, Martin C. Michel, Thomas Steckler. 1st ed. 2020. Springer Nature 2020 Cham : Springer International Publishing : Imprint: Springer, 2020. 1 online resource (X, 423 p. 34 illus., 21 illus. in color.) text txt rdacontent computer c rdamedia online resource cr rdacarrier Handbook of Experimental Pharmacology, 0171-2004 ; 257 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. 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. Description based on publisher supplied metadata and other sources. English Pharmacology. Neurosciences. Cardiology. Oncology . Pharmacology/Toxicology. https://scigraph.springernature.com/ontologies/product-market-codes/B21007 Neurosciences. https://scigraph.springernature.com/ontologies/product-market-codes/B18006 Cardiology. https://scigraph.springernature.com/ontologies/product-market-codes/H33037 Oncology. https://scigraph.springernature.com/ontologies/product-market-codes/H33160 Pharmacology/Toxicology Neurosciences Cardiology Oncology Pharmacology Neuroscience Internal Medicine reproducibility study design data analysis data reporting data integrity quality management open access Cardiovascular medicine Bespalov, Anton. editor. edt http://id.loc.gov/vocabulary/relators/edt Michel, Martin C. editor. edt http://id.loc.gov/vocabulary/relators/edt Steckler, Thomas. editor. edt http://id.loc.gov/vocabulary/relators/edt Handbook of Experimental Pharmacology ; 257 |
language |
English |
format |
eBook |
author2 |
Bespalov, Anton. Bespalov, Anton. Michel, Martin C. Michel, Martin C. Steckler, Thomas. Steckler, Thomas. |
author_facet |
Bespalov, Anton. Bespalov, Anton. Michel, Martin C. Michel, Martin C. Steckler, Thomas. Steckler, Thomas. |
author2_variant |
a b ab a b ab a b ab m c m mc mcm m c m mc mcm t s ts t s ts |
author2_role |
HerausgeberIn HerausgeberIn HerausgeberIn HerausgeberIn HerausgeberIn HerausgeberIn |
author_sort |
Bespalov, Anton. |
title |
Good Research Practice in Non-Clinical Pharmacology and Biomedicine / |
spellingShingle |
Good Research Practice in Non-Clinical Pharmacology and Biomedicine / Handbook of Experimental Pharmacology, 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. |
title_full |
Good Research Practice in Non-Clinical Pharmacology and Biomedicine / edited by Anton Bespalov, Martin C. Michel, Thomas Steckler. |
title_fullStr |
Good Research Practice in Non-Clinical Pharmacology and Biomedicine / edited by Anton Bespalov, Martin C. Michel, Thomas Steckler. |
title_full_unstemmed |
Good Research Practice in Non-Clinical Pharmacology and Biomedicine / edited by Anton Bespalov, Martin C. Michel, Thomas Steckler. |
title_auth |
Good Research Practice in Non-Clinical Pharmacology and Biomedicine / |
title_new |
Good Research Practice in Non-Clinical Pharmacology and Biomedicine / |
title_sort |
good research practice in non-clinical pharmacology and biomedicine / |
series |
Handbook of Experimental Pharmacology, |
series2 |
Handbook of Experimental Pharmacology, |
publisher |
Springer Nature Springer International Publishing : Imprint: Springer, |
publishDate |
2020 |
physical |
1 online resource (X, 423 p. 34 illus., 21 illus. in color.) |
edition |
1st ed. 2020. |
contents |
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. |
isbn |
3-030-33656-5 |
issn |
0171-2004 ; |
callnumber-first |
R - Medicine |
callnumber-subject |
RM - Therapeutics and Pharmacology |
callnumber-label |
RM1-950 |
callnumber-sort |
RM 11 3950 |
illustrated |
Not Illustrated |
dewey-hundreds |
600 - Technology |
dewey-tens |
610 - Medicine & health |
dewey-ones |
615 - Pharmacology & therapeutics |
dewey-full |
615 615.1072 |
dewey-sort |
3615 |
dewey-raw |
615 615.1072 |
dewey-search |
615 615.1072 |
oclc_num |
1143621169 |
work_keys_str_mv |
AT bespalovanton goodresearchpracticeinnonclinicalpharmacologyandbiomedicine AT michelmartinc goodresearchpracticeinnonclinicalpharmacologyandbiomedicine AT stecklerthomas goodresearchpracticeinnonclinicalpharmacologyandbiomedicine |
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n |
ids_txt_mv |
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carrierType_str_mv |
cr |
hierarchy_parent_title |
Handbook of Experimental Pharmacology, 257 |
hierarchy_sequence |
257 |
is_hierarchy_title |
Good Research Practice in Non-Clinical Pharmacology and Biomedicine / |
container_title |
Handbook of Experimental Pharmacology, 257 |
author2_original_writing_str_mv |
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