Verified clinical trials


Verified Clinical Trials is a global research subject database registry dedicated to improving clinical trial safety and data quality by preventing dual enrollment and protocol violations. Created by physicians and research professionals with over 50 years of experience, it aims to enhance patient safety, ensure data integrity, and reduce study costs through innovative verification solutions including biometric fingerprint and facial recognition technologies. The company collaborates with sponsors, CROs, and research sites worldwide to promote ethical and efficient clinical research. It actively participates in industry events, partners with research centers, and develops solutions to prevent duplicate research subjects, including professional patients, across all phases of clinical trials.

Industries

clinical-trials
health-care
medical

Nr. of Employees

small (1-50)

Verified clinical trials


Patents

Method for creating and using registry of clinical trial participants

US-11568963-B2

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Products

Research subject registry platform

Cloud-hosted platform that stores participant enrollment-status records and supports identity verification, cross-study matching, and managed participant communications under configurable privacy controls.


Services

Cloud-based registry service that verifies participant enrollment status across studies at screening and provides ongoing monitoring during study conduct to prevent duplicate enrollment and related protocol violations.

Optional biometric identity verification deployed on-site or remotely via mobile and web interfaces, producing encrypted templates for identity matching without storing raw biometric images.

Managed program to permit secure, privacy-controlled contact with enrolled or registry participants for safety notifications, dissemination of results, and recruitment opt-ins while maintaining privacy controls.

Analytics and reporting on site-level screening, enrollment, screen-fail, and early-termination metrics to inform site selection and improve enrollment efficiency.

Online tools and consulting to estimate financial impact and cost savings from preventing duplicate subjects and protocol violations, supporting procurement and deployment decisions.

Technical and commercial integration services with clinical-trial automation platforms, CRO partners, and research sites to embed registry checks into recruitment and enrollment workflows.

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Expertise Areas

  • Research subject registry management and cross-study duplicate detection
  • Biometric identity verification for clinical research
  • Decentralized and remote participant verification workflows
  • Privacy-preserving cross-sponsor data sharing and participant communications
  • Show More (4)

Key Technologies

  • Biometric fingerprint recognition
  • Facial recognition
  • Encrypted biometric template generation
  • Mobile and web-based verification applications
  • Show More (4)

News & Updates

VCT participates in the ADA annual meeting to showcase solutions for safeguarding data integrity in diabetes, obesity, and GLP-1 therapies.

Discussion on the challenges posed by professional patients attempting to enroll in multiple trials simultaneously.

Explains the verification process and technologies used to prevent duplicate enrollment.

Details the risks and costs associated with duplicate subjects and how VCT mitigates these issues.

VCT leads efforts to prevent duplicate enrollment at the American Society of Clinical Psychopharmacology annual meeting.

VCT achieved international standards for information security management, reinforcing data security and integrity.


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