Join the session using the link: Zoom Link

Objectives

After participating in this educational activity, attendees should be able to:
1| Summarize the OHRP and FDA requirements for human subjects research training.

2| Distinguish how CITI training achieves part of the federal requirements.

3| Describe the terms therapeutic misconception and clinical equipoise as they relate to ethical conduct of research.

Presenter(s): 

Susan Garrow-Sloan, RN, CCRP

Education and Quality Assurance (EQA) Specialist
Baystate Health