sIRB regulations and policies have been announced and implemented to help address the challenges of conducting clinical trials involving multiple research sites.| Advarra
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
This checklist offers a comprehensive framework for managing all necessary essential regulatory documents efficiently.| Advarra
A formal hazard communication or IBC SOP is critical to ensure clinical personnel understand the risks involved with genetically engineered investigational products.| Advarra
Advarra leverages exceptional client service, innovative technology and robust global regulatory expertise. Check out our blog for more industry insights.| Advarra