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VCT To Exhibit at World Vaccine Congress

Vaccine clinical trials pose unique challenges with regards to duplicate research subjects or professional subjects. Typically, large numbers of subjects are dosed at the first visit in a vaccine clinical trial. There is no way for a site or principal investigator to adequately check if the research subject is a duplicate or professional subject. Subjects …

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The Professional Research Subject Problem In Clinical Trials

Clinical research patients are compensated for their participation in clinical trials. In some therapeutic areas and types of clinical trials, the compensation for enrolling in one or more clinical trials or at multiple research sites is enough to influence patients to join more than one contemporaneously and expose themselves to multiple investigational products or multiple …

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RESEARCH SITES AND SPONSORS COOPERATE TO PREVENT PROFESSIONAL RESEARCH SUBJECTS IN CNS CLINICAL TRIALS BY USING VERIFIED CLINICAL TRIALS

Duplicate subjects, or what is known as professional research subjects, exist in most clinical trials to varying degrees. CNS clinical trials are especially prone to duplicate subjects or over enrollment in clinical tials. The issue exists from phase 1 healthy volunteer studies to multiple phase 2/3 clinical trials across many therapeutic indications. Use of global …

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Strategies To Proactively Detect And Prevent Professional Research Subjects With Verified Clinical Trials Research Subject Database Registry

Clinical trials around the world face challenges from professional research subjects or dual enrollment in clinical trials. One group of subjects that have high rates of participation in clinical research are subjects who enroll in multiple trials for the purpose of generating income through study payments or using clinical trials as medical care. These subjects …

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Professional Research Subject Detection Now A Clinical Trial Essential

After more than a decade in the business of detecting “professional research subjects,” Verified Clinical Trials is a familiar name to stakeholders across the research enterprise—including the nefarious players who ride-share from city to city in search of unprotected sites where they can enroll in studies purely for the financial gain. It’s an underappreciated underground …

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Prevent Professional Research Subjects With The VCT Global Research Subject Database: European Snapshot

A quick look at some screening data in 3 close European countries demonstrates how research subjects travel to screen concurrently at multiple different sites. Professional research subjects often travel large distances between states or countries to do so. Some travel is within the same country to different sites, but there is significant travel between countries. …

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Verified Clinical Trials and Remote and Virtual Clinical Trials. Preventing Professional Research Subjects With A Global Database Registry

Conducting virtual clinical trials or remote clinical trials, or just a standard clinical trial? Verify your research subject’s eligibility and ensure they are not concurrently enrolling in multiple clinical trials at once. Verified Clinical Trials eliminates professional research subjects or duplicate research subjects. This can be accomplished completely off site with our newest technology. Avoid …

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Prevent Professional Research Subjects With Verified Clinical Trials

Professional research subjects cause issues with placebo rates, data quality and safety.  The issue is more common than most would think.  Upwards of 10% of research subjects will attempt to enroll in more than one clinical trial concurrently or before a safe and mandatory wash out period has occurred. Without a tool like Verified Clinical …

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Verified Clinical Trials Offers Virtual Clinical Trial Solution To Prevent Co-Enrollment or Duplicate Subjects

Conducting virtual or remote clinical trials? Verify your research subjects eligibility and ensure they are not concurrently enrolling in multiple clinical trials at once. Avoid co-enrollment in clinical trials or duplicate subjects in clinical trials as well as protocol violations. Select better quality subjects for your trial so that you can meet her in points …

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