Join the session using this link: Zoom Link

Objectives

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

1| Compare the federal regulations and submission requirements for exempt, expedited, and full board research.

2| Manage the IRB submission process by distinguishing between package types, locating submission documents, and successfully submitting through IRB Net.

3| Perform follow-on submissions such as amendments, continuing reviews, and study closures according to regulatory requirements.

Presenter(s): 

Anne Marie Mal, MDiv, CIM
IRB Analyst
Baystate Health

L. Cliff Rhodes, MBA, CIM, CIP
IRB Regulatory Specialist
Baystate Health

NameRoleFinancial Relationship DisclosuresDiscussion of
Unlabeled/Unapproved Uses of
Drugs/Devices in Presentation?
Anne Marie Mal, MDiv, CIMSpeaker/AuthorNo relevant relationships with ineligible companies to disclose 
L. Cliff Rhodes, MBA, CIM, CIPSpeaker/AuthorNo relevant relationships with ineligible companies to disclose 
Session date: 
05/21/2025 - 2:00pm EDT to 06/21/2025 - 3:00pm EDT
Location: 
Zoom
MA
United States
See map: Google Maps
Add to calendar: 
  • 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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