I JUST SUBMITTED TO THE IRB… WHAT NOW?

HAVE I REALLY SUBMITTED IT?? (NOT IN THIS CASE - CLICK THE YELLOW BOX)

CLICK ON THE ROUTING ASSIGNMENT LIST ICON

YOU HAVE NOT CLICKED “SAVE AND CONTINUE” TO BEGIN ROUTING

SIGNATURES ARE STILL NEEDED: “WAITING FOR PI SIGNOFF”

SIGNATURES ARE STILL NEEDED: “IN PROCESS” VS. “COMPLETED”

CHECK TO SEE WHETHER THE IRB HAS RECEIVED IT

YES! I DID IT!

AFTER AN IRB ANALYST IS ASSIGNED, HOW DO I TRACK IT?

CLICK “TRACK LOCATION”

OK, THIS IS WHOM I SHOULD CALL WITH QUESTIONS.

REVIEWERS HAVE COMPLETED THEIR REVIEWS

I NEED TO RESPOND TO THE IRB! CLICK TO OPEN FROM YOUR “INCOMPLETE TASKS”

OR: GO TO “PROJECT ASSISTANT,” THEN TO “MY PROJECTS”

UNDER “REQUEST TYPE,” CLICK THE HYPERLINK

PI RESPONSE FORM

SCROLL DOWN TO REVIEW PROVISOS

SCROLL DOWN TO REVISE APPLICATION & CLICK ON THE GREEN BAR

CLICK “ADD REVISION” IN ORDER TO EDIT YOUR APPLICATION

IF YOU SEE “SAVE AND CONTINUE,” YOU CAN EDIT YOUR APPLICATION

DON’T FORGET TO CHECK THE BOX BEFORE CLICKING “SAVE ATTACHMENTS”!

CHECK TO ENSURE THE NEW VERSION SHOWS UP UNDER GREEN BAR

CLICK ON THE GREEN BAR TO REVISE YOUR CONSENT FORM

CLICK “ADD REVISION” IN ORDER TO EDIT YOUR CONSENT FORM

CLICK “CHECK-OUT DOCUMENT”

A POP-UP WINDOW WILL ASK YOU TO OPEN OR SAVE

CLICK “SAVE”

DON’T FORGET TO CLICK “COMPLETE CHECKOUT”

AFTER EDITING, CLICK “CHECK-IN DOCUMENT”

BROWSE AND SAVE YOUR EDITED CONSENT FORM

DON’T FORGET TO CHECK THE BOX BEFORE CLICKING “SAVE ATTACHMENTS”!

CHECK TO ENSURE THE NEW VERSION SHOWS UP UNDER GREEN BAR

ANSWER THE 3 QUESTIONS IN THE PI RESPONSE FORM BEFORE SAVING & ROUTING

I HAVE RECEIVED APPROVAL! YOU CAN FIND YOUR LETTER IN “PROJECT CORRESPONDENCE” OR “SUBMISSIONS HISTORY”

YOUR LETTER IN “PROJECT CORRESPONDENCE”

YOUR LETTER IN “SUBMISSIONS HISTORY”

CLICK ON “ADD NEW FORM” TO CREATE A FORM 2 FOR REVISION

SCREEN 1 OF THE FORM 2 - JUST ANSWER AND CLICK “SAVE AND CONTINUE”

THINGS TO REMEMBER AFTER SUBMITTING AN APPLICATION TO THE IRB Form 1 (new application): Gently remind your investigators and department chairs to sign off. Form 1 (new application): Gently remind your investigators and department chairs to sign off. Don’t forget to save all the way through the routing pages. Don’t forget to save all the way through the routing pages. Check your workflow tracking to make sure the IRB received your submission. Check your workflow tracking to make sure the IRB received your submission. If you have questions, look up your analyst and call her. If you have questions, look up your analyst and call her. Provisos can be found in your letter (project correspondence or submissions history) or in the PI Response form. Provisos can be found in your letter (project correspondence or submissions history) or in the PI Response form. You/your sponsor can disagree with a proviso; call and let’s talk about it! You/your sponsor can disagree with a proviso; call and let’s talk about it!

THINGS TO REMEMBER AFTER SUBMITTING AN APPLICATION TO THE IRB In your PI Response form, remember to check the box to the left of your revised application and consent form before you save that page. In your PI Response form, remember to check the box to the left of your revised application and consent form before you save that page. Visit our website: Getting Started page, iMedRIS guides, FAQs, policies, and more! Visit our website: Getting Started page, iMedRIS guides, FAQs, policies, and more! Check the deadline schedule for full Board submissions - submit 3 weeks in advance. Check the deadline schedule for full Board submissions - submit 3 weeks in advance. In general, a full Board submission will be returned to you with recommendations about 1 ½ weeks before the meeting. In general, a full Board submission will be returned to you with recommendations about 1 ½ weeks before the meeting. Exempt applications: expect a response in 5-7 business days. Exempt applications: expect a response in 5-7 business days. Expedited applications: expect a response within 2 weeks. Expedited applications: expect a response within 2 weeks. All correspondence from iMedRIS goes directly to your UT address! All correspondence from iMedRIS goes directly to your UT address!

THINGS TO REMEMBER ONCE YOUR APPLICATION HAS BEEN APPROVED ANY CHANGE (even minor) to your study must be reviewed and approved by the IRB before the change is implemented. ANY CHANGE (even minor) to your study must be reviewed and approved by the IRB before the change is implemented. Remember to submit adverse events and major protocol deviations to the IRB for review. Remember to submit adverse events and major protocol deviations to the IRB for review. If your study is expedited or full Board (check your IRB #), you must submit a continuation/renewal form (Form 3) every year, 3 weeks before your expiration date. If your study is expedited or full Board (check your IRB #), you must submit a continuation/renewal form (Form 3) every year, 3 weeks before your expiration date. You cannot enroll above the number of subjects approved for your study - a subject is considered enrolled after signing a consent form, even if they drop out or do not pass screening tests. You cannot enroll above the number of subjects approved for your study - a subject is considered enrolled after signing a consent form, even if they drop out or do not pass screening tests. The consent form must be signed by the PI within 72 hours of the subject and person obtaining consent signing it. The consent form must be signed by the PI within 72 hours of the subject and person obtaining consent signing it.