دانلود کتاب تحقیق بالینی و بهداشت و درمان آکسفورد
Oxford Handbook of Clinical and Healthcare Research, 1ed

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.

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Contents

۱ Research: why and how?
۲ Navigating research methods: basic concepts in biostatistics and epidemiology
۳ Navigating research methods: quantitative and clinical/epidemiological methods
۴ Navigating research methods: qualitative methods
۵ Navigating research methods: evidence-based medicine (EBM)
۶ Navigating research methods: critical appraisal
۷ Navigating research methods: clinical audit
۸ Setting the scene and ICH GCP in clinical and healthcare research
۹ Informed consentin a research setting
۱۰ Ethics of clinical and healthcare research: general considerations, Mental Capacity Act, Human Tissue Act
۱۱Role and responsibilities: investigator and research team
۱۲ Role and responsibilities of the sponsor
۱۳ Monitoring
۱۴ Clinical trial design
۱۵ Clinical trial protocols: study protocol
۱۶ Data capture tools: case report form (CRF)
۱۷ Clinical trial supplies: investigational medicinal products (IMPs)
۱۸ IMP accountability
۱۹ Safety reporting
۲۰ Data management
۲۱ Research project management
۲۲ Essential documents
۲۳ Archiving
۲۴ Audits and inspections
۲۵ Fraud and misconduct
۲۶ Authorship
۲۷ Publication process
۲۸ Start-up toolkit: from funding an idea, through implementation, to achieving an impact