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

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 ...

Note to researchers: Protocols submitted after 4 PM on Fridays (or the last business day of the week) will be reviewed the following week by the IRB Analysts. The IRB Analysts make efforts to review ...

Unless instructed otherwise, please make sure you have the following items to include with your application: consent/assent form (IRB Form 3.1) any written instruments, sample questions, and/or other ...

Furthermore, attention must be given to the cultural context and local regulations. IRB Approval must be granted PRIOR to study beginning. Your protocol must be submitted to the W&M IRB at least 4 ...

The IRB Module provides a streamlined way for researchers to create and submit protocols for studies involving human subjects. It provides support for initial submissions, modifications, reportable ...

It is important for researchers to understand how to use an external IRB as the IRB of record, as well as what is required throughout the process. This UB CTSI Watch and Learn educational module video ...

The IRB is a federally mandated committee that provides ethical oversight for all research involving human subjects. All scholarship and research that involves humans, whether funded or unfunded, must ...

If you plan to conduct research on human subjects, you will need to work with CU Boulder’s Institutional Review Board (IRB). The purpose of the IRB is to help ensure that human subject research is ...