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E-grāmata: Oxford Handbook of Clinical and Healthcare Research

Edited by (Senior Medical Advisor/Clinician Scientist at the Medical Research Council (Human Nutrition Research); Chair of UK Need for Nutrition Education/Innovation Programme (NNEdPro), Cambridge University Hospitals/School of Clinical Medicine), Edited by , Edited by , Edited by , Edited by
  • Formāts: 640 pages
  • Sērija : Oxford Medical Handbooks
  • Izdošanas datums: 03-Mar-2016
  • Izdevniecība: Oxford University Press
  • Valoda: eng
  • ISBN-13: 9780191502958
  • Formāts - PDF+DRM
  • Cena: 35,68 €*
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  • Formāts: 640 pages
  • Sērija : Oxford Medical Handbooks
  • Izdošanas datums: 03-Mar-2016
  • Izdevniecība: Oxford University Press
  • Valoda: eng
  • ISBN-13: 9780191502958

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The Oxford Handbook of Clinical and Healthcare Research is a practical, concise, and easy-to-use reference for the full range of clinical and healthcare research topics, while incorporating evidence based medicine. Comprehensively providing a wide breadth of knowledge, this handbook clearly covers both the qualitative and quantitative aspects.

This handbook includes clear instructions on the legislative requirements as well as the practical requirements of commissioning, conducting, analysing, and reporting research for those in clinical or healthcare practice, education or training. This book has been written with Good Clinical Practice (GCP) education in mind, giving valuable information needed for the accredited certificates and diploma-level benchmark exams now commonly required by employers.

Whether you need practical advice on setting up and running a trial, negotiating regulations, learning vital research skills, or to study the underpinning concepts of research methods, this handbook will give you the vital information, clinical evidence, and guidance you need.

Recenzijas

The Oxford Handbook of Clinical and Healthcare Research packs a lot of information into a literally hand-sized ... book, with precise writing." * Norman M. Goldfarb, Journal of clinical research best practises * A unique handbook that covers all the stages of clinical research along with a clear description of the regulations / processes that current researchers need to comply with. This truly addresses a much needed gap in the various research handbooks. * Dr Puja Myles, Associate Professor Health Protection and Epidemiology; Nottingham University *

Contributors xiii
Symbols and abbreviations xv
1 Research: why and how?
1(18)
2 Navigating research methods: basic concepts in biostatistics and epidemiology
19(20)
3 Navigating research methods: quantitative and clinical/epidemiological methods
39(18)
4 Navigating research methods: qualitative methods
57(18)
5 Navigating research methods: evidence-based medicine (EBM)
75(4)
6 Navigating research methods: critical appraisal
79(12)
7 Navigating research methods: clinical audit
91(10)
8 Setting the scene and ICH GCP in clinical and healthcare research
101(24)
9 Informed consent in a research setting
125(18)
10 Ethics of clinical and healthcare research: general considerations, Mental Capacity Act, Human Tissue Act
143(26)
11 Role and responsibilities: investigator and research team
169(16)
12 Role and responsibilities of the sponsor
185(46)
13 Monitoring
231(34)
14 Clinical trial design
265(32)
15 Clinical trial protocols: study protocol
297(20)
16 Data capture tools: case report form (CRF)
317(22)
17 Clinical trial supplies: investigational medicinal products (IMPs)
339(28)
18 IMP accountability
367(24)
19 Safety reporting
391(16)
20 Data management
407(12)
21 Research project management
419(14)
22 Essential documents
433(20)
23 Archiving
453(16)
24 Audits and inspections
469(28)
25 Fraud and misconduct
497(18)
26 Authorship
515(10)
27 Publication process
525(18)
28 Start-up toolkit: from funding an idea, through implementation, to achieving an impact
543(28)
Index 571