A clinical trials manual from the Duke Clinical Research Institute : lessons from a horse named Jim /
Saved in:
Main Author: | |
---|---|
Corporate Author: | |
Other Authors: | |
Format: | Book |
Language: | English |
Published: |
Chichester, West Sussex, UK ; Hoboken, NJ :
Wiley-Blackwell,
2010.
|
Edition: | 2nd ed. |
Subjects: | |
Online Access: | Publisher description Table of contents only Contributor biographical information |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Table of Contents:
- Lessons from a horse named Jim and other events in history affecting the regulation of clinical research
- The process : developing new drugs, biologics, and devices
- Good clinical practice and the regulations
- Informed consent and the regulations
- Institutional review boards
- Adverse events and unanticipated problems involving risks to subjects and others
- Monitoring, audits, and inspections
- The principal investigator, the clinical research coordinator, and the study site
- The protocol
- Study feasibility : reviewing a specific protocol
- Study activities
- Study documents/essential documents
- Management of study drugs, biologics, and devices
- Managing clinical trial data
- Global health and international trials.