• Detecting duplicate subjects, professional patients, and other protocol violations at the time of screening.

• Verifying each participant’s prior clinical trial history to ensure full compliance with inclusion/exclusion criteria.

• Improving data quality by eliminating unqualified or repeat participants.

• Reducing placebo response rates by excluding subjects who attempt to enroll in multiple studies simultaneously.

• Protecting participant safety by ensuring proper washout and non-overlapping exposure to investigational products.

• Saving time and costs associated with failed endpoints, study restarts, and extended timelines.

VCT is the only solution that provides cross-sponsor visibility into a subject’s research history — giving sponsors the confidence that their trials are built on accurate data, qualified participants, and sound science.