Contract Research Organizations (CROs) are essential partners in the execution of clinical trials, managing critical functions such as site activation, patient recruitment, data collection, monitoring, and regulatory compliance.
Verified Clinical Trials (VCT) collaborates closely with CROs around the world to enhance study quality, efficiency, and compliance. By integrating VCT’s global research subject database into the clinical trial workflow, CROs can confidently ensure that every subject enrolled is verified, eligible, and unique.
VCT removes the burden of detecting duplicate and professional subjects by proactively verifying participants at the time of screening, identifying 17+ preventable protocol violations derived from inclusion and exclusion criteria. This not only improves participant safety and data quality but also reduces regulatory scrutiny and protocol deviations—ultimately strengthening study outcomes and accelerating timelines.
Working hand-in-hand with CROs, VCT delivers a seamless layer of protection across trials, sites, and therapeutic areas—ensuring cleaner data, greater operational consistency, and safer, more compliant research.