‏241.00 ₪

Oxford Handbook of Clinical and Healthcare Research

‏241.00 ₪

ISBN13

9780199608478

מהדורה

1st ED

הוצאה לאור

Oxford

פורמט

Paperback

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.

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.

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פרטים

מידע נוסף

מידע נוסף
מהדורה	1st ED
פורמט	Paperback
הוצאה לאור	Oxford
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
Author	Edited by Sumantra Ray, Sue Fitzpatrick, Rajna Golubic, Susan Fisher, and edited with assistance of Sarah Gibbings