Federal requirements have shifted to require most multisite clinical trials to rely on a single IRB (sIRB) for trial oversight.| Advarra
Recent regulations and policies have many institutions establishing policies and processes for working with an external sIRB. Read more:| Advarra
Get resources and best practices for clinical research reporting requirements including common rule, FWA, ALCOA, and more.| Advarra
Get resources and best practices for clinical research operations including site management, workflows, community engagement, and more.| Advarra
Get resources and best practices for clinical research compliance including 21 CFR Part 11, regulatory management, FWA, and more.| Advarra