The University IRB uses consultants to supplement IRB review when a specific project requires expertise beyond the scope of IRB membership. For example, a project/package may require: scientific or ...

Single IRB Review is an arrangement in which one institution's IRB provides review, approval and oversight for the Human Research activities of multiple institutions. This is intended to streamline ...

UAB is one of over 600 institutions that have joined SMART IRB. SMART IRB stands for "Streamlined, Multisite, Accelerated Resources for Trials". SMART IRB is an IRB reliance model designed to ...

Occasionally, protocols require investigators or other institutions to rely on one another to perform an IRB review. Please see this guidance if wanting more information about Individual Investigator ...

These collected resources can help when you're developing IRB protocols and related materials. If you have further questions after reviewing these materials, please contact our office. We also ...

Collaborative Institutional Training Initiative (CITI) is a consortium of Universities and institutions to distribute federally funded training content to meet regulatory compliance. All applicants, ...

Projects/packages requiring Full Committee Review must be determined to be complete before these are placed on the agenda for review at a scheduled IRB meeting. Project/packages requiring ...

Click's IRB module will replace IRBNET for all UB researchers. This new system will simplify and improve your protocol submission and approval process. All Continuing Renewals will need to be ...

At the outset of the project students and partners should discuss and put in writing agreements with regard to the ownership of data and the guidelines and restrictions put upon students by the ...

Following the completion of HRPP initial training, UAB HRPP policy requires refresher training once every three years for key personnel involved in human subjects research. All training courses are ...

The Food and Drug Administration announced last week that it would not regulate “IRB shopping,” a practice in which sponsors of clinical trials choose to submit proposed research to institutional ...