Appropriate for all research personnel, pharmacists, nurses, physicians, and administrators
Learning Objectives:
- Describe the history and purpose of clinical trials
- Describe important ethical and regulatory aspects of conducting research
- Discuss the role of the investigator and the institution when engaged in human subjects research
- Identify the components of a research protocol
- Discuss eligibility and patient safety once on study
- Describe data management requirements for clinical trials
- Discuss practical issues of conducting clinical trials in the outpatient setting
- Discuss compliant billing practices
- Describe best practices in investigational agent management
For questions please contact Lynda Owen.
Lynda.owen@duke.edu or 919-257-8164
Joint