Join the session using this link: Zoom Link

Objectives

After participating in this educational activity, attendees should be able to:

1| Differentiate between Human Subjects Research and Non-Human Subjects Research to determine what requires IRB oversight versus IRB documentation.

2| Identify activities that qualify as Non-Human Subjects Research based on regulatory criteria.

3| Describe the process of submitting a project in IRBNet by selecting the appropriate package type, locating submission documents, and completing the submission process.

Presenter(s): 

Anne Marie Mal, MDiv, CIM
IRB Analyst
Baystate Health