IRB Policy 15.1 Update

IRB Standard Operating Policies and Procedures

IRB Tips/Tools/Research Links

IRB Meeting Dates and Deadlines

Electronic IRB Submissions/ARIA

IRB Forms and Reference Materials

IRB Committee Rosters

Update of IRB Standard Operating Policy 15.1: Elements of Informed Consent Documents and Process

In an effort to streamline processes for the IRB and for Clinical Trials operations, IRB Policy 15.1 concerning written consent was modified to allow flexibility in the standard consent language. The language offered in the policy is now "suggested" instead of mandatory. Please let Tim Atkinson know if you have any other suggestions (tnatkinson@uams.edu).