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Beschreibung
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.
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.
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.
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.
Über den Autor
Sumantra Ray, Senior Medical Advisor/Clinician Scientist; Chair, Medical Research Council (Human Nutrition Research); UK Need for Nutrition Education/Innovation Programme (NNEdPro), Cambridge University Hospitals/School of Clinical Medicine, Sue Fitzpatrick, Director; Former Head of Education and Training, Redtree People and Sue Fitzpatrick Training; Institute of Clinical Research, Rajna Golubic, Gates Scholar; Trust Doctor, Medical Research Council and University of Cambridge (Epidemiology Unit and St. John`s College), West Suffolk Hospital, UK, Susan Fisher, Research Manager, Medical Research Council (Human Nutrition Research), Cambridge, UK
Inhaltsverzeichnis
- 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
Details
| Erscheinungsjahr: | 2016 |
|---|---|
| Fachbereich: | Therapie |
| Genre: | Importe, Medizin |
| Rubrik: | Wissenschaften |
| Medium: | Taschenbuch |
| Reihe: | Oxford Medical Handbooks |
| Inhalt: | Kartoniert / Broschiert |
| ISBN-13: | 9780199608478 |
| ISBN-10: | 0199608474 |
| Sprache: | Englisch |
| Einband: | Blätter |
| Autor: |
Ray, Sumantra
Fitzpatrick, Sue Golubic, Rajna Fisher, Susan Gibbings, Sarah |
| Redaktion: |
Golubic, Rajna
Gibbings, Sarah Fitzpatrick, Sue Ray, Sumantra Chair of UK Need for Nutrition Education/Innovation Programme (NNEdPro) Fisher, Susan |
| Hersteller: |
Oxford University Press
Oxford Medical Handbooks |
| Verantwortliche Person für die EU: | Deutsche Bibelgesellschaft, Postfach:81 03 40, D-70567 Stuttgart, vertrieb@dbg.de |
| Maße: | 183 x 105 x 25 mm |
| Von/Mit: | Rajna Golubic (u. a.) |
| Erscheinungsdatum: | 03.05.2016 |
| Gewicht: | 0,32 kg |
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