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The electronic IRB submission process is used by eMedicus, Inc.
to provide and facilitate a paperless process for the review and
approval of research protocols. Paper copies are also accepted.
All the required forms are available and able to be completed on-line. The
staff at eMedicus will review all materials and forms for completeness and accuracy
and prepare materials for the IRB meeting. In accordance with the Code of Federal
Regulations Title 21 CFR 56 and Title 45 CFR 46, the IRB committee will meet
to review the research proposals.
The IRB Committee meets on a weekly basis and more frequently if
needed. All investigators/sponsors/CROs will be notified of the
IRB Committee's decision within 24 hours by telephone and/or email.
A detailed letter from the IRB Committee to the investigator will
be sent by U.S. mail or FedEx.
To obtain additional information, please fill out the form
and we will contact you to discuss how eMedicus can assist you with
your IRB needs.
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