Healthwise

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.

Due to the threat of the COVID-19 (Coronavirus), we are taking precautionary measures to protect our staff and patients. We are implementing a temporary NO VISITOR policy at this time. Only patients or patients and their guardians will be allowed into the office. Please note, this is not to inconvenience anyone! The virus is a very real threat and it is essential that we stay healthy in order to provide needed care for our patients. If you are sick, we ask that you CALL the office to speak with a nurse before you come in. The nurse will provide specific instructions for you. Please DO NOT enter the office if you are sick (upper respiratory symptoms, fever, cough, or flu like symptoms). We are closely monitoring the situation and will update you as circumstances change. Thank you for your understanding!!