Writing clinical research protocols ethical considerations /
I tiakina i:
| Kaituhi matua: | |
|---|---|
| Kaituhi rangatōpū: | |
| Ētahi atu kaituhi: | |
| Hōputu: | Tāhiko īPukapuka |
| Reo: | Ingarihi |
| I whakaputaina: |
Burlington, MA ; London :
Elsevier Academic,
c2006.
|
| Ngā marau: | |
| Urunga tuihono: | An electronic book accessible through the World Wide Web; click to view |
| Ngā Tūtohu: |
Tāpirihia he Tūtohu
Kāore He Tūtohu, Me noho koe te mea tuatahi ki te tūtohu i tēnei pūkete!
|
Rārangi ihirangi:
- Introduction to the art and science of clinical research
- What you need to know about clinical research ethics
- What you need to know about the regulation of clinical research
- Designing a clinical research study
- Selecting subjects for clinical studies
- Risks and benefits in clinical research
- Recruiting subjects
- Informed consent
- Privacy and confidentiality
- The "ethics" section
- Procedures and methods
- Statistics, data collection and management, and record keeping
- Use of human biological materials
- Special issues raised by evolving areas of clinical research
- Case histories : learning from experience.