UTRGV SOM What you need to know about the IRB & Human Subjects Research

The Institutional Review Board (IRB) reviews human subjects research for compliance with federal regulations and institutional policies with the aim of protecting the rights of participants. Gaining IRB approval is an important step in study start-up but often there is a good deal of confusion about when IRB review is required and what the IRB is looking for when they review a study. This can lead to unnecessary frustration and delays in getting IRB approval. The purpose of this session is to provide a transparent overview of the IRB process to demystify the process.
At the conclusion of the session, you should have a better understanding of:
•    Identify when IRB review is required.
•    Describe the criteria for approval of human subjects’ research study.
•    Recognize best practices for completing an IRB application.

Tuesday, October 12, 2021 at 12:00pm to 1:00pm

Virtual Event
Event Type

Training & Development

Target Audience

Faculty

Location

Virtual Event

Tags

Mentoring Program, Medical Educator Series, General Faculty Development

Group
Office of Faculty Affairs - SOM, School of Medicine
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