To add a user, condition, or drug to eIRB, click the appropriate hyperlink above to access the web form to request the data be added. Once this form is submitted and verified, you will be notified that the data has been added to eIRB. If you have any questions or need further assistance, please contact the IRB office at firstname.lastname@example.org or 508-856-4261.
***ALL SPONSOR REQUESTS must be SUBMITTED through the OnCore Clinical Trial Management Systems Process. Please use form (CTMS-103a).
***New Users: After requesting user acces, click on the Banner for step-by-step guidance on how to
"Get Started" with the IRB application process.