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The Professional Research Subject And The Effect On Placebo Rates And Adverse Events. The Use Of The Verified Clinical Trials Research Subject Database


Verified Clinical Trials
Verified Clinical Trials (VCT), the global research subject clinical trials database registry to prevent dual enrollment in clinical research trials provides clinical trial sponsors, research sites, and CROs a comprehensive tool to improve their study safety and data. Leveraging their powerful technology and proprietary software, Verified Clinical Trials is able to reduce professional research subjects from screening and entering a trial that they do not belong in.  Subjects that are currently enrolled in another study will be determined ineligible and identified prior to costly and time consuming recruitment and screening efforts. Verified Clinical Trials 

offers a completely scalable web based system without the need for any hardware or installation ever.  In this manner Verified Clinical Trials is able to reach and enlist all research subjects and site users instantly. 

Verified Clinical Trials is dedicated to reducing protocol violations in clinical trials while improving clinical trial safety and data quality. Verified Clinical Trials will stop dual enrollment in clinical trials and prevent professional research subjects from enrolling in to the trials you conduct. While all therapeutic areas are at risk for this issue, CNS trials including pain, psychiatric and substance abuse have some of the attempted highest dual enrollment rates. The Verified Clinical Trials research subject clinical trials database registry is well established in both early and late phase trials.

If a research subject screen fails at one site in many instances they will attempt to screen at another site armed with the proper knowledge to gain entry to the trial.  “This is not the research subject that you want in your clinical trials” stated Mitchell Efros MD FACS CEO of Verified Clinical Trials . The Verified Clinical Trials system is able to exclude subjects that screen fail elsewhere or were involved with the same protocol or the same investigational product.  “The Verified Clinical Trials system is much more than just a system to stop dual enrollment” added Kerri Weingard ANP, COO of Verified Clinical Trials. “This solution actually is a tool to reduce many protocol deviations”.

Never before has there been a tool like Verified Clinical Trials that enables clinical trial sponsors to protect against dual enrollment in clinical trials.  Attempts at manual review of limited personal identifying information retrospectively is limited in it it’s scope and ability to track these professional research subjects and prevent multiple simultaneous enrollments.  Additionally, by using Verified Clinical Trials, the research site will stop the poor quality subject PRIOR to a costly screening saving even more money as well as protecting their data. Verified Clinical Trials will not only protect dual enrollment within your company’s trial, but will catch subjects currently screening or enrolled in other trials across all therapeutic areas and all phases of clinical trials.

Verified Clinical Trials is a forward thinking company developed by experts active in the clinical research community to proactively improve research subject safety and data quality in clinical research trials.

Verified Clinical Trials has presented at numerous conferences and is recognized as an industry thought leader.  Upcoming meetings include the ISCTM, ACPU, DIA, ASCPT, and Outsourcing Clinical Trials East as well as many others.Verified Clinical Trials halts dual enrollment in clinical trials and defines itself as the world’s leader in the field of database registries in clinical trial research. Verified Clinical Trials is the only clinical research database registry designed specifically to enhance the quality of both early and late phase trials and has the scalability to reach all sites nationally as well as on a global level. Verified Clinical Trials offers numerous other value added services to the clinical research site, CRO, and Pharmaceutical Sponsor, that prove invaluable with regards to financial and legal issues and liabilities. For more information, RSVP to or visit