Health Sciences and Minimal Risk IRBs, IRB News / Volume 7, Number 2, February 2015
Campus policy requires new IRB applications be submitted for ongoing studies every five years, except in certain cases. These replacement applications should be submitted as a new initial review application in ARROW and at least 3 months (for non –VA studies) or 5 months (for VA studies) prior to expiration of the original application. To assist study teams in complying with this policy, a new guidance document on [Link for document 46546 is unavailable at this time.] is now available
This guidance document clarifies that replacement applications need to include a document called the Study Status Summary. Beginning March 2, 2015, a study status summary will be required for all replacement applications. To assist with review of the replacement application, this document will need to describe the following key aspects of study progress:
As always, if you have any questions about this new guidance, please do not hesitate to contact us via any of the avenues noted below.
As announced in the October newsletter, the HS
IRBs office launched a pilot quality improvement project. The goal of this project is to reach out to study teams whose applications may be stalled in the review process.
Since beginning the project, nearly 300 emails have been sent to study teams and approximately 30% of study teams have responded to these outreach efforts. Although this is fairly high response rate, the HS IRBs office encourages any study team receiving these emails to be in touch with us. Knowing about unforeseen delays study teams are experiencing (e.g., funding delays, workload issues, etc.) during the IRB review process helps the HS IRBs office manage its review load more efficiently and improve turnaround times. We also are happy to assist study teams who encounter difficulties during the pre-review process and to provide guidance on next steps.
If you have any questions about this
project, please email firstname.lastname@example.org.
The HS IRBs office is again offering the IRB for Beginners Workshop. The 90-minute workshop is held in the HSLC computer lab and gives participants a first-hand look at resources available on the HS-IRBs website as well as tips for working with the ARROW submission system. The workshop also introduces participants to the IRB review process. This workshop is designed to help people who are new to the HS-IRBs review process.
This workshop is scheduled for the following dates:
Registration is required and space is limited. Please email email@example.com to reserve your spot and include any questions or topics you would like addressed during the workshop.
ARROW Outage February 28th
ARROW will be unavailable Saturday, February 28th from 1PM to 5PM for upgrades and maintenance. We apologize for any inconvenience.
The Office of the Vice Chancellor for Research and Graduate Education will be launching a Post-Approval Monitoring Program in March 2015. The Post-Approval Monitoring Program will expand the efforts of the Human Research Protection Program (HRPP) in providing education and guidance for investigators who have received Institutional Review Board (IRB) approval. The PAM Program is designed to improve the quality of research on campus and maximize protections for participants. The PAM Program is separate from the IRB offices on campus.
Under the PAM Program, active, non-exempt studies may be selected randomly for routine monitoring. After a study has been selected for monitoring, the PAM Program will notify the study team and
schedule an initial visit. At this initial visit, the monitor
will go over the study with the study team and provide an opportunity to ask
any questions about the review process. During the monitoring visit, the
monitor will review study materials and be available to the study team for questions. Study teams will then receive a report of observations from their
If you have questions about the PAM Program, please contact Ryan Moze (firstname.lastname@example.org).
Whether you have a question about a specific protocol, a general question about the submission process, or need clarification about research policy, we have several ways you can reach us.