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Get Started With Schulman

On this page, you’ll find the information you need to get started with Schulman IRB. Need a hand? Don’t hesitate to call us at 513-761-4100.

If you represent a sponsor/CRO, please review how to Submit Study as a Sponsor.

If you are submitting an investigator-initiated study, please review how to Submit Study as a Site.

Schulman IRB has IRB meetings every day of the business week, with special submission deadlines for Phase I and Canadian-based research.

Full Board Review Submission Deadlines

Submission deadline is one week prior to intended meeting.

Meeting deadlines website 11-29-15

Protocols that involve no greater than minimal risk to human subjects may qualify for Minimal Risk Review.

Please review Turnaround Time information to learn more about Schulman’s review timelines for specific submissions.

If you represent a research site that is part of a multi-site study, please review how to Submit Site.

If you are a sponsor/CRO representative submitting on behalf of a site, please review how to Submit Site as a Sponsor.

Most sites are reviewed daily via expedited review.

Please review Turnaround Time information to learn about common submission issues that can delay the review of your site.

If you represent a sponsor/CRO, please reference Ongoing Review for Sponsors.
If you represent a research site, please reference Ongoing Review for Sites.

To review Schulman’s expectations for investigator education and responsibilities, please reference investigator’s Responsibilities.

Use eSubmission to quickly and securely submit your materials.

Need to learn about Schulman’s current fees for service? Request Fee Schedule.

You can monitor the progress of your submission and download approval documents in real time using Schulman’s industry-leading Part-11 compliant electronic tools. Need to learn about Schulman’s electronic tools? Request WebPortal 3D Demo.

Need more help? Contact Us.