Western IRB (WIRB) is a commercial IRB under contract with Saint Louis University (SLU) to review eligible industry-sponsored, multi-center clinical trials. WIRB is the only central IRB that SLU investigators may submit to at this time. SLU is currently opening the WIRB process to divisions that have completed WIRB 101 training.
• Is an industry-sponsored, multi-center clinical trial
• Has already been pre-reviewed or approved by WIRB (submitted by sponsor or another site)
• Is being submitted by an authorized department or division
• Procedures take place at an authorized site (currently SLU or SLU Hospital)
• Is not an HUD
• SLU investigators do not hold the IND or IDE
• Study was not previously reviewed by SLU IRB
How do I get access to WIRB's system?
Investigators and regulatory support staff planning to submit to WIRB should request access to the WIRB Net system (WIRB's electronic submission system) as soon as possible. This can be done on WIRB's website: www.wirb.com. Having WIRB Net access will be necessary to submit to WIRB.
What steps do I take to submit to WIRB?
Step 1: Confirm that a study is eligible for WIRB review. Contact WIRB Client Services (firstname.lastname@example.org) to determine whether WIRB has the protocol (ask whether there is a WIRB protocol ID for that sponsor protocol). If they have, then review SLU eligibility criteria, above, to ensure submission to WIRB is allowable. Investigators are encouraged to consult with the SLU IRB to make eligibility determinations. Inquiries can be sent to email@example.com or call the IRB office at 314-977-7744.
Step 2a: Investigator begins local processes necessary for all clinical trials at SLU. To get approval for submission to WIRB, the Clinical Trial Agreement (CTA) must be agreed upon and other necessary financial requirements must be met (for details, contact the Clinical Trials Office at 977-6335 or firstname.lastname@example.org). Note that the signed 1572 and signed Tenet application must be submitted with the CTA for the Tenet review process, if applicable.
When preparing study budgets, IRB fees should be included. There is a one-time SLU administrative review fee of $750 for WIRB studies which will be billed to the research department with the expectation that the sponsor ultimately provides payment. WIRB review fees are available here. (Note: SLU may not have the most current version.) WIRB will bill the sponsor directly if the sponsor allows it. Some sponsors require all billing to go through the SLU research division. If sponsors do not pay WIRB invoices in a timely manner, WIRB will bill the SLU department for payment.
All investigators listed on the study must also have annual disclosures on file with the conflict of interest office and must have completed training in human subjects research protections.
Step 2b: Prepare the WIRB Submission Authorization Form (SLU form) along with required attachments and submit to the SLU IRB office. The SLU IRB office facilitates the SLU administrative review process; submission to WIRB cannot occur until the Submission Authorization Form is approved. This process may occur concurrently with work on the CTA and financial arrangements.
Note that the following will be required for the SLU Administrative Review Process:
• Completed WIRB Submission Authorization Form (SLU form)
• Completed WIRB Submission Form for Multi-Center Protocols (the WIRB application)
- This electronic WIRB form is completed in the WIRB Net system and should be saved as a PDF and printed for submission to SLU IRB prior to submitting the application to WIRB.
• Sponsor's protocol, any recruitment material, Investigator's Brochure
• Consent or Assent Documents previously approved by WIRB (WIRB can provide copy)
- SLU investigators will not be responsible for generating the SLU consents/assents. SLU has given WIRB required language for SLU consents, and any protocol specific language will be provided to WIRB as an appendix to the signed WIRB Submission Authorization Form. WIRB staff will generate SLU consents/assents accordingly.
• HIPAA Documents
- SLU investigators will be responsible for drafting HIPAA Authorization Forms. Please use the standard SLU template HIPAA Authorization Form when preparing this document, and remember to attach it to your WIRB application when you ultimately submit.
The SLU IRB office will route materials to other SLU offices as needed (Clinical Trials Office, General Counsel, Radiation Safety, Biological Safety, Conflict of Interest, etc.) for review. However, if investigators are aware that approvals will be necessary from other offices or committees, they are encouraged to work with these groups directly as soon as possible to expedite processes.
If issues arise during SLU Administrative Review, the PI or study contact will be contacted and revisions may be requested.
Step 3: Submission to WIRB. Once SLU authorization (the signed WIRB Submission Authorization Form) is received, the investigator can proceed with submission of materials directly to WIRB. The SLU Authorization Form with Appendix C should be included with the WIRB submission, along with the SLU approved HIPAA Authorization form. The WIRB website can be referenced for assistance in submitting materials (www.wirb.com).
Step 4: WIRB Review. WIRB will contact the investigator/contact person directly with questions about the submission, and with determinations of approval or disapproval. Once approved, all approval documents will be sent to the investigator. SLU IRB is copied on all correspondence. NOTE: WIRB will hold approvals for 3 days to allow SLU administrators time to verify that the consent document contains all necessary information prior to release to investigators.
Step 5: Do not commence research until all institutional approvals are in place. Make sure that all institutional approvals and the clinical trial agreement are in place prior to beginning the study.
What do I need to do after approval?
WIRB and Saint Louis University each have responsibilities for overseeing this research, thus there are reporting requirements to both organizations.
SUBMISSIONS TO WIRB AFTER INITIAL APPROVAL:
Investigators should submit subsequent protocol documents, events or activities directly to WIRB according to guidelines provided by WIRB. Submissions to WIRB include:
• Protocol Amendments
• Continuing Review Requests
• Unanticipated Problems (may or may not also be an SAE)
• Safety reports or other event reports from sponsors that are not submitted to WIRB by the sponsor on the investigator's behalf
• Closure Notifications
• Other submissions required by WIRB
SLU IRB will be notified by WIRB about SLU investigators' submission activity, thus there is no current requirement to provide copies of these types of WIRB submissions to SLU IRB. However, if there are proposed amendments to local sections of the study (personnel, local consent language, etc.), investigators may opt to consult with SLU IRB in advance of submitting to WIRB to avoid situations of WIRB approving, but SLU not approving the changes. See contact info, below.
SUBMISSIONS TO SLU IRB AFTER INITIAL APPROVAL:
To ensure appropriate institutional oversight of research activities, investigators should directly notify SLU IRB of the following events on WIRB protocols:
• SAEs that are not UPs (and thus not reported to WIRB)
• Subject complaints
• Breaches of confidentiality
• Audit notifications
• Monitor reports if not submitted to WIRB
Submit the above items in accordance with definitions and submission requirements detailed in the SLU IRB Requirements for Reporting Events Relating to Subjects/Subject Safety. SLU IRB will route information related to these reports to university officials as needed for review; however, investigators should also contact General Counsel and/or the SLU Privacy Officer when appropriate.
Who should I contact if I have questions?
Questions about the WIRB process and SLU requirements should go to Susan George at email@example.com or 314-977-7741.
Questions regarding WIRB submission and WIRB reporting requirements are best handled by contacting WIRB directly or by visiting www.wirb.com.