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Global CRO Drives Study Startup Efficiency by Converting Local IRB Sites to Central IRB Review
Research sites that rely on a local IRB typically take at least twice as long to activate than sites that rely on the study’s single central IRB. Utilizing the central IRB not only helps to streamline study startup but also enables increased efficiencies in managing sites throughout the study’s lifecycle.
In collaboration with Advarra, PRA Health Sciences improved processes and substantially improved the ratio of sites able to use Advarra as the central IRB. This improved startup timelines and saved money for PRA’s sponsor clients, ultimately speeding the drug development process and getting therapies to patients more quickly.
Find out more—download our free case study Global CRO Drives Study Startup Efficiency by Converting Local IRB Sites to Central IRB Review.
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