Under FDA regulations, an IRB is an appropriately constituted group that has been formally designated to review and monitor biomedical research involving human subjects. In accordance with FDA regulations, an IRB has the authority to approve, require modifications in (to secure approval), or disapprove research. The Community Medical Centers Institutional Review Board (IRB) is an administrative body established, both in advance and by periodic review, that ensures appropriate steps are taken to protect the rights and welfare of humans participating as subjects in research.
All IRB submissions to the Community Medical Centers IRB will be completed through the electronic submission software system referred to as CyberIRB. Please be aware that CyberIRB has built-in hard-stops therefore, incomplete submission will be automatically returned to Investigators. Prospective or current researchers can refer to the electronic system CyberIRB to complete the IRB application. If you need access to the CyberIRB system, please contact the IRB at [email protected]