Virtual Regulatory Binder: Instructions

Last revised: 

How to Use the Binder

The Virtual Regulatory Binder is comprised of sections that apply to the range of human research studies. To access, click on the tabs at the left of each page.

Each section outlines the regulatory requirements, institutional policies and Good Clinical Practice (GCP) guidelines for organization, recordkeeping, QIU tips, and links to additional resources (e.g., federal regulations, IRB policies and forms, HUB tools).

For additional guidance on establishing a regulatory binder refer to the Regulatory Binder Instructions.

Whom to Contact for Help

The QIU provides individual consultation and educational offerings to both new and experienced members of the research community, including investigators and study staff. To schedule a binder consultation, please email the IRB

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