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‏239.00 ₪
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Oxford Handbook of Clinical and Healthcare Research

‏239.00 ₪
ISBN13
9780199608478
זמן אספקה
21 ימי עסקים
תאריך יציאה לאור
3 במרץ 2016
  • Reflects the latest legislative framework
  • Provides equal focus to qualitative and quantitative aspects
  • Covers the breadth of information required for GCP education and related examination, including FPH
  • Comprehensive start-up toolkit for new researchers in any health-related field
  • App available from the App Store, Google Play, and MedHand Bookstore.
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The Oxford Handbook of Clinical and Healthcare Research is an evidence-based, succinct, and easy-to-use reference for the full range of clinical and healthcare research topics. Providing a wide breadth of essential knowledge, this comprehensive text takes the researcher through the steps from general good clinical practice in healthcare research to the process and management of research.

This handbook includes clear instructions on the legislative and practical requirements of commissioning, conducting, analysing, and reporting research for those in clinical or healthcare practice, education, or training. Written with Good Clinical Practice (GCP) education in mind, it includes valuable information needed for the accredited certificates and diploma-level benchmark exams now commonly required by employers. This is a definitive text for all clinical and healthcare research students, as well as graduates with an interest in clinical and healthcare research.

מידע נוסף
תאריך יציאה לאור 3 במרץ 2016
תוכן עניינים

1:Research - How and Why
2:Basic concepts in biostatistics and epidemiology
3:Quantitative and clinical / epidemiological methods
4:Qualitative methods
5:Evidence Based Medicine (EBM)
6:Critical appraisal
7:Clinical Audit
8:Setting the scene and ICH-GCP in clinical and healthcare research
9:Informed consent in a research setting
10:Ethics of clinical and healthcare research: general considerations, Mental Capacity Act, Human Tissue Act
11:Role and Responsibilities: Investigators and Research Team
12:Role and Responsibilities: Sponsor
13:Monitoring
14:Clinical Trial Design
15:Clinical Trial Protocols: Study Protocol
16:Data Capture Tools: Case Report Form (CRF)
17:Clinical Trial Supplies: IMPs
18:IMP Accountability
19:Safety Reporting
20:Data management
21:Research Project Management
22:Essential Documents
23:Archiving
24:Audits and Inspections
25:Fraud and Misconduct
26:Authorship
27:Publication process
28:Start-up toolkit: from funding an idea, through implementation, to achieving an impact
זמן אספקה 21 ימי עסקים