東華大學圖書館 |

語系: 繁體中文

說明(常見問題)

回圖書館首頁

手機版館藏查詢

登入

回首頁

切換: 標籤 | MARC模式 | ISBD

Good research practice in non-clinic...

Bespalov, Anton.

FindBook

Google Book

Amazon

博客來

Good research practice in non-clinical pharmacology and biomedicine

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Good research practice in non-clinical pharmacology and biomedicine/ edited by Anton Bespalov, Martin C. Michel, Thomas Steckler.
其他作者:	Bespalov, Anton.
出版者:	Cham :Springer International Publishing : : 2020.,
面頁冊數:	x, 423 p. :ill., digital ;24 cm.
內容註:	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.
Contained By:	Springer eBooks
標題:	Drugs - Research. -
電子資源:	https://doi.org/10.1007/978-3-030-33656-1
ISBN:	9783030336561

Good research practice in non-clinical pharmacology and biomedicine
Good research practice in non-clinical pharmacology and biomedicine[electronic resource] /edited by Anton Bespalov, Martin C. Michel, Thomas Steckler. - Cham :Springer International Publishing :2020. - x, 423 p. :ill., digital ;24 cm. - Handbook of experimental pharmacology,v.2570171-2004 ;. - Handbook of experimental pharmacology ;v.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.

Open access.

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.

ISBN: 9783030336561

Standard No.: 10.1007/978-3-030-33656-1doiSubjects--Topical Terms:

685164
Drugs
--Research.

LC Class. No.: RS122 / .G663 2020

Dewey Class. No.: 615.1072

Good research practice in non-clinical pharmacology and biomedicine
LDR:02762nmm a2200349 a 4500 001 2216013
003 DE-He213
005 20200707133839.0
006 m d
007 cr nn 008maaau
008 201120s2020 sz s 0 eng d
020 $a 9783030336561 $q (electronic bk.)
020 $a 9783030336554 $q (paper)
024 7 $a 10.1007/978-3-030-33656-1 $2 doi
035 $a 978-3-030-33656-1
040 $a GP $c GP
041 0 $a eng
050 4 $a RS122 $b .G663 2020
072 7 $a MMG $2 bicssc
072 7 $a MED071000 $2 bisacsh
072 7 $a MKG $2 thema
082 0 4 $a 615.1072 $2 23
090 $a RS122 $b .G646 2020
245 0 0 $a Good research practice in non-clinical pharmacology and biomedicine $h [electronic resource] / $c edited by Anton Bespalov, Martin C. Michel, Thomas Steckler.
260 $a Cham : $b Springer International Publishing : $b Imprint: Springer, $c 2020.
300 $a x, 423 p. : $b ill., digital ; $c 24 cm.
490 1 $a Handbook of experimental pharmacology, $x 0171-2004 ; $v v.257
505 0 $a 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.
506 $a Open access.
520 $a 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.
650 0 $a Drugs $x Research. $3 685164
650 1 4 $a Pharmacology/Toxicology. $3 890953
650 2 4 $a Neurosciences. $3 588700
650 2 4 $a Cardiology. $3 861477
650 2 4 $a Oncology. $3 751006
700 1 $a Bespalov, Anton. $3 3448015
700 1 $a Michel, Martin C. $3 1532569
700 1 $a Steckler, Thomas. $3 1244752
710 2 $a SpringerLink (Online service) $3 836513
773 0 $t Springer eBooks
830 0 $a Handbook of experimental pharmacology ; $v v.257. $3 3448016
856 4 0 $u https://doi.org/10.1007/978-3-030-33656-1
950 $a Biomedical and Life Sciences (Springer-11642)