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Institutional review board (IRB) - OBGYN Associates
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Our Health Library information does not replace the advice of a doctor. Please be advised that this information is made available to assist our patients to learn more about their health. Our providers may not see and/or treat all topics found herein.

Institutional review board (IRB)

An institutional review board (IRB) is an independent committee made up of medical and nonmedical members, such as physicians, statisticians, and community advocates. It ensures that a clinical trial is ethical and that the rights of study participants are protected.

All institutions that conduct or support biomedical research involving people, by U.S. government regulation, must have an IRB that initially approves and periodically reviews the research.

An IRB reviews and approves protocols, informed-consent forms, physician credentials and eligibility, and other patient materials. The role of an IRB is to work closely with the U.S. Food and Drug Administration (FDA) to make sure that patient safety is the main priority of a clinical trial.

Current as of: October 24, 2023

Author: Ignite Healthwise, LLC Staff

Clinical Review Board
All Healthwise education is reviewed by a team that includes physicians, nurses, advanced practitioners, registered dieticians, and other healthcare professionals.