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  Research Participants  

Participants in research are a precious resource to clinical advancement. Human subject research is a privilege, not a right. Consistent with this philosophy, the mission of Harrison Independent Review Board (IRB) is to provide that the rights and welfare of human subjects are protected.

There are various research-related sites that can provide additional information regarding your participation in research studies. Please choose the following links:

The Food and Drug Administration is responsible for protecting the public health by assuring safety, efficacy and security of human drugs.

OHRP is an organization that provides leadership for the protection of volunteers in research that is conducted or supported by the US Department of Health and Human Services (DHHS).

Centerwatch is an organization that provides information used by patients, pharmaceutical companies and research centers involved in clinical research around the world. For more information about participating in a clinical trial, select the link below “Participating in a Clinical Trial” to review a short Q&A overview of some questions you may have about research.

Participating in a Clinical Trial



Contact Harrison IRB
As a participant in research, if you feel that your rights have been violated or you would like to report misconduct at a site, you can contact Harrison IRB by phone at (740) 845 0814 or email at info@harrisonirb.com

Serious Adverse Event

  If you have contacted this site to report a Serious Adverse Event, please call the study doctor listed in the Informed Consent document for the study in which you are participating or dial 911.