At Quorum Review IRB, we know that every study has its unique set-up challenges. The site approval process is complex enough—the last thing you need is frustration due to vague communication about your IRB approval process.

Quorum has put a great deal of effort into streamlining our approval processes and forms to gather all the information needed to conduct a thorough review without burdening the study site with excessive paperwork. We respond quickly and communicate clearly in a straightforward and helpful way. Our goal is to make the approval process as simple and frustration-free as possible.

Initial Study Site Submission

Information on how to set up a study with Quorum IRB for fast and efficient approval.

Study Site Changes

Information on which research study site changes require submission to Quorum IRB for approval and which do not.

Periodic Review and Closure

Information on study site periodic review, study site status report forms and FAQs.

Study Site Safety Reporting

Information about Quorum IRB study site safety reporting guidelines, forms, and safety reporting FAQs.

Participant Recruitment

Guidelines for clinical research sites on creating and submitting recruitment materials.


Common questions and information to help study sites avoid obstacles.

Working with Institutions

Quorum Review IRB has built out many processes to better accommodate the unique needs of institutions.

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