IBISResearch: IRB

IRB Module is a core component of the Huron Research Suite, designed to streamline and automate the management of human subjects research protocols. It supports compliance with federal regulations and institutional policies while improving operational efficiency.

System Access

IBISResearch: IRB

About

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  • Getting Started

    All active UM Researchers are automaticaly provided access to our Huron's IRB Module.

    If you are sponsoring an individual not affiliated with UM, yet requires access to IBISResearch, you must submit a Research Suite Access form

    Research Suite Access

  • Resources

    This system training is required for all individuals who participate in the design, conduct, and/or reporting of FDA research as a prerequisite to utilizing the system. Completion will be monitored to ensure compliance with the 21 CFR Part 11 regulatory training requirement.

    System Training

Support

Our Research Support Helpdesk is here to help: 

Monday - Friday
8:00 AM - 5:00 PM
305-243-2314		 Submit Request

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