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Clinical Research Education Series (CRES) | “External IRB & Reliance Agreements"
This presentation will provide a brief overview of updates and changes within the Office of Research Protections. It will provide useful information regarding: Overview of the External IRB Roles and Responsibilities, Requirements for Establishing Reliance Utilizing an External IRB, Future Changes & Updates to the Current Workflow and additional information.
Target Audience
Employees at Houston Methodist Hospital Research Institute
Learning Objectives
Participant Learning Outcomes:
- Overview of the External IRB roles and responsibilities
- Explanation of the regulatory requirements for establishing reliance when utilizing an External IRB
- Outline of the current process for submitting an External IRB submission
- Discuss future changes/updates to the current workflow
- Gather input from research teams to assist in process restructuring workflow
Virtual - ZOOM link with be provided to the registered participants.
Presenter Info:
- Leola Griffin, BS, CIP
- Prince Agyapong
- Amber Cumpian
1.00 Attendance
Available Credit
- 1.00 Attendance
For Houston Methodist Employees:
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- Update your mobile number.
If you have previously created a profile, you may proceed with registering for the activity by selecting “Log In.” Select “Visitor Log In,” and login with the information you previously used.
For additional information please visit the FAQ section.