Join the session using the link: Zoom Link
Objectives
After participating in this educational activity, attendees should be able to:
1| Define what an Institutional Review Board (IRB) is: Explain the role of the IRB in protecting the rights, welfare, and safety of human research participants.
2| Describe what the Baystate Health IRB does: Understand how the IRB reviews research protocols, assesses risk, and evaluates informed consent.
3| Review the Baystate IRB review workflow: Summarize the major steps from submission → review → determination → ongoing oversight.
4| Recognize who serves on the Baystate Health IRB: Describe the required composition of an IRB, including scientific, non-scientific, and unaffiliated (community) members.
Presenter(s):
Michael Boland, CIM
IRB Coordinator
Baystate Health
| Name | Role | Financial Relationship Disclosures | Discussion of Unlabeled/Unapproved Uses of Drugs/Devices in Presentation? |
|---|---|---|---|
| Michael Boland | Speaker/Author | No relevant relationships with ineligible companies to disclose | No |
- 1.00 AMA PRA Category 1 Credit™
- 1.00 ANCC Contact Hours
- 1.00 BCIPE Risk Management
- 1.00 IPCE Credit Hour(s)
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