The Office of Research Integrity and Center for Clinical and Translational Science will be providing a repeat hands on workshop on informed consent regulatory requirements.
ORI is pleased to announce that the streamlining feature promised in the April 17, 2018 announcement has been put into production sooner than anticipated!
Since E-IRB has been put into production, ORI has received feedback indicating preparation of the application by study support-staff is cumbersome due to the multiple points at which the Principal Investigator (PI) is required to log-in to E-IRB and perform a PI-only task.
The Office of Research Integrity and Center for Clinical and Translational Science will be providing a hands on workshop on informed consent regulatory requirements.