We have nearly 50 years of combined clinical, therapeutic and regulatory experience as well as technology and process‑related insights.
50% OF ALL FDA APPROVALS SINCE 2013
15K+ STUDIES SUPPORTED
5M+ PATIENTS TO DATE
MINIMIZE RISK AND UNCERTAINTY SO YOU CAN MOVE AHEAD QUICKLY WITH CONFIDENCE
In clinical research, every detail matters. As trial complexity increases, new risks emerge. Missteps and inaccurate data can mean more expensive trials and delays in bringing life-saving treatments to the patients who need them most. We help you spot risks before they become problems to avoid costly delays.