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Submit a Study

Sponsors​Submit a Multisite Study

A Sponsor/CRO requesting review of a new multisite protocol that has never been reviewed by Schulman must submit:

And, if applicable:

​Submit a Single Site Study

A Sponsor/CRO requesting review of a new multisite protocol that has never been reviewed by Schulman must submit:

  • Single Site Study Submission Form or Minimal Risk Single Site Submission Form
  • Protocol
  • Template Informed Consent Document(s) (Microsoft Word format required)
  • Curriculum Vitae (CV) of Principal Investigator/Qualified Investigator (PI/QI) and each Sub-Investigator (Sub-I), if not already on file – CVs must reflect experience, be signed and dated within the past 2 years.
    • Sub-I CVs are not generally required for site submissions on studies that have been qualified by the Board as minimal risk and/or non-interventional.

And, if applicable:

 

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

Assignment to a Board meeting is dependent upon the complete and accurate submission of all required documents. Refer to Federally Funded/FWA Study, Submitting a Device Study and Transfer of IRB Oversight for Study for additional requirements for these types of study submissions.

Please note: Full Board review of studies with Canadian sites are reviewed only at Friday Board meetings.