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Beschreibung
This handbook is a definitive, up-to-date, and succinct text covering the legislative requirements, scientific foundations, and clinical good practice necessary for clinical, academic, and healthcare research.
This handbook is a definitive, up-to-date, and succinct text covering the legislative requirements, scientific foundations, and clinical good practice necessary for clinical, academic, 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 |
| 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 |
| Maße: | 183 x 105 x 25 mm |
| Von/Mit: | Rajna Golubic (u. a.) |
| Erscheinungsdatum: | 03.03.2016 |
| Gewicht: | 0,32 kg |
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 |
| 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 |
| Maße: | 183 x 105 x 25 mm |
| Von/Mit: | Rajna Golubic (u. a.) |
| Erscheinungsdatum: | 03.03.2016 |
| Gewicht: | 0,32 kg |
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