Small to mid-size IRBs or predominantly SBER IRBs can encounter challenges and constraints when faced with that first clinical trial. Hear from institutional experts on how to set up the basic framework needed for reviewing this type of research, including creating opportunities within the current policies to remain compliant, reduce risk, and establish monitoring for clinical research.
Learning Objectives:
Discuss the basic requirements for reviewing a clinical trial
Share strategies and tools for the monitoring and oversight of your first clinical trial
Consider benefits of ceding review to an external IRB or using IRB experts